Food Standards: Requirements for Substitute Standardized Meat and Poultry Products Named by Use of an Expressed Nutrient Content Claim and a Standardized Term, 33803-33819 [05-11493]
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Federal Register / Vol. 70, No. 111 / Friday, June 10, 2005 / Rules and Regulations
(1) Send the producer a maturity
notice letter before MAL maturity.
(2) Maintain the MAL or LDP
documents according to FSA
requirements.
(3) Transmit the necessary funds to
repay the MAL to FSA.
(b) FSA shall process the CCC release
of paper receipts or EWR’s where such
a release is appropriate.
§ 1421.422
Inspections and reviews.
The books, documents, papers, and
records of the DMA and parent
company shall be maintained for six
years after the applicable crop year and
shall be made available to CCC for
inspection and examination at all
reasonable times. At any time after an
application is received, CCC shall have
the right to examine all books,
documents, papers, and determine
whether the DMA is operating or has
operated in accordance with the
regulations in this part, any articles of
incorporation, articles of association,
partnership documents, agreements
with producers, the representations
made by the DMA in its application for
approval, and, where applicable, its
agreements with CCC. If the DMA is
determined to be not complying with
this part or any of its agreements, CCC
will take appropriate action as provided
in elsewhere in this subpart or other
action CCC determines appropriate.
§ 1421.423
Appeals.
Parts 11 and 780 of this title apply to
this subpart.
Signed in Washington, DC, on May 25,
2005.
James R. Little,
Executive Vice President, Commodity Credit
Corporation.
[FR Doc. 05–11505 Filed 6–9–05; 8:45 am]
BILLING CODE 3410–05–P
DEPARTMENT OF AGRICULTURE
Animal and Plant Health Inspection
Service
9 CFR Part 94
[Docket No. 04–091–2]
Addition of Malaysia To List of
Regions in Which Highly Pathogenic
Avian Influenza Subtype H5N1 Is
Considered To Exist
Animal and Plant Health
Inspection Service, USDA.
ACTION: Affirmation of interim rule as
final rule.
AGENCY:
SUMMARY: We are adopting as a final
rule, without change, an interim rule
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that amended the regulations
concerning the importation of animals
and animal products by adding
Malaysia to the list of regions in which
highly pathogenic avian influenza
(HPAI) subtype H5N1 is considered to
exist. We took that action to prevent the
introduction of HPAI subtype H5N1 in
the United States.
DATES: The interim rule became
effective on August 7, 2004.
FOR FURTHER INFORMATION CONTACT: Dr.
Julie Garnier, Staff Veterinarian,
Technical Trade Issues Team, National
Center for Import and Export, VS,
APHIS, 4700 River Road Unit 39,
Riverdale, MD 20737–1231; (301) 734–
5677.
SUPPLEMENTARY INFORMATION:
Background
Highly pathogenic avian influenza
(HPAI) is an extremely infectious and
fatal disease of poultry and a wide
variety of other birds. HPAI can strike
poultry quickly without any infection
warning signs and, once established, the
disease can spread rapidly from flock to
flock. In some instances, strains of HPAI
viruses can be infectious to people.
Human infections with AI viruses under
natural conditions have been
documented in recent years. Particularly
alarming is the HPAI strain of most of
these outbreaks, H5N1, which has
crossed the species barrier and caused
severe disease, with high mortality, in
humans. Recent outbreaks of HPAI in
Southeast Asia have caused significant
concern among health authorities
worldwide because of the potential for
the human and avian flu viruses to swap
genes, creating a new virus to which
humans would have little or no
immunity.
The Animal and Plant Health
Inspection Service (APHIS) of the
United States Department of Agriculture
(USDA or the Department) regulates the
importation of animals and animal
products into the United States to guard
against the introduction of animal
diseases. The regulations in 9 CFR parts
93, 94, and 95 (referred to below as the
regulations) govern the importation of
certain animals, birds, poultry, meat,
other animal products and byproducts,
hay, and straw into the United States in
order to prevent the introduction of
various animal diseases, including HPAI
subtype H5N1.
In an interim rule effective August 7,
2004, and published in the Federal
Register on February 1, 2005 (70 FR
5043–5044, Docket No. 04–091–1), we
amended the regulations in part 94 by
adding Malaysia to the list of regions in
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33803
§ 94.6(d) where HPAI subtype H5N1
exists.
Comments on the interim rule were
required to be received on or before
April 4, 2005. We received one
comment by that date, from a private
citizen. The commenter supported the
interim rule.
Therefore, for the reasons given in the
interim rule and in this document, we
are adopting the interim rule as a final
rule without change.
This action also affirms the
information contained in the interim
rule concerning Executive Order 12866
and the Regulatory Flexibility Act,
Executive Order 12988, and the
Paperwork Reduction Act.
Further, for this action, the Office of
Management and Budget has waived its
review under Executive Order 12866.
List of Subjects in 9 CFR Part 94
Animal diseases, Imports, Livestock,
Meat and meat products, Milk, Poultry
and poultry products, Reporting and
recordkeeping requirements.
PART 94—RINDERPEST, FOOT-ANDMOUTH DISEASE, FOWL PEST (FOWL
PLAGUE), EXOTIC NEWCASTLE
DISEASE, AFRICAN SWINE FEVER,
CLASSICAL SWINE FEVER, AND
BOVINE SPONGIFORM
ENCEPHALOPATHY: PROHIBITED
AND RESTRICTED IMPORTATIONS
Accordingly, we are adopting as a final
rule, without change, the interim rule
that amended 9 CFR part 94 and that was
published at 70 FR 5043–5044 on
February 1, 2005.
I
Done in Washington, DC, this 6th day of
June 2005.
Elizabeth E. Gaston,
Acting Administrator, Animal and Plant
Health Inspection Service.
[FR Doc. 05–11504 Filed 6–9–05; 8:45 am]
BILLING CODE 3410–34–P
DEPARTMENT OF AGRICULTURE
Food Safety and Inspection Service
9 CFR Parts 319 and 381
[Docket No. 92–024F]
Rin 0583–AC82
Food Standards: Requirements for
Substitute Standardized Meat and
Poultry Products Named by Use of an
Expressed Nutrient Content Claim and
a Standardized Term
Food Safety and Inspection
Service, USDA.
ACTION: Final rule.
AGENCY:
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Federal Register / Vol. 70, No. 111 / Friday, June 10, 2005 / Rules and Regulations
SUMMARY: The Food Safety and
Inspection Service (FSIS) is amending
the Federal meat and poultry products
inspection regulations to establish a
general definition and standard of
identity for standardized meat and
poultry products that have been
modified to qualify for use of an
expressed nutrient content claim in
their product names. These products
will be identified by an expressed
nutrient content claim, such as ‘‘fat
free,’’ ‘‘low fat,’’ and ‘‘light,’’ in
conjunction with an appropriate
standardized term, e.g., ‘‘low fat
bologna.’’ FSIS is taking this action to:
Assist consumers in maintaining
healthy dietary practices by providing
for modified versions of standardized
meat and poultry products that have
reductions of certain constituents that
are of health concern to some
consumers, such as fat, cholesterol, and
sodium; increase regulatory flexibility
and support product innovation, and
provide consumers with an informative
nutrition labeling system.
DATES: This final rule will be effective
January 1, 2008, the uniform
compliance date for all meat and
poultry products subject to labeling
regulations issued by FSIS between
January 1, 2005 and December 31, 2006.
However, establishments may begin to
produce meat and poultry products in
compliance with this final rule anytime
before the effective date.
FOR FURTHER INFORMATION CONTACT: Dr.
Robert Post, Director, Labeling and
Consumer Protection Staff, Office of
Policy, Program, and Employee
Development, Food Safety and
Inspection Service, U.S. Department of
Agriculture, Washington, DC 20250–
3700; (202) 205–0279.
SUPPLEMENTARY INFORMATION:
Background
On December 29, 1995, FSIS
published a proposed rule in the
Federal Register to amend the Federal
meat and poultry products inspection
regulations to establish a general
definition and standard of identity (the
‘‘general standard’’) for standardized
meat and poultry products that have
been modified to qualify for use of an
expressed nutrient content claim in
their product names (60 FR 67474).
Under the proposed general standard,
meat and poultry products with a
regulatory standard of identity or
composition in 9 CFR Parts 319 and
381, subpart P, would be permitted to be
formulated and processed with
ingredients otherwise not provided for,
or in amounts greater than, that allowed
by the standard in order to qualify for
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certain expressed nutrient content
claims permitted in 9 CFR 317 subpart
B and 381, subpart Y, such as ‘‘fat free,’’
‘‘low fat,’’ and ‘‘light.’’ Instead of being
identified as ‘‘substitute’’ standardized
meat and poultry products, as required
by the current regulations (9 CFR
317.313(d) and 381.413(d)),
standardized meat and poultry products
formulated or processed in accordance
with the proposed general standard
could be identified by an expressed
nutrient content claim in conjunction
with the standardized term.
To allow modified versions of
standardized meat and poultry products
that have been formulated to reduce
their fat content to be marketed without
having to be labeled as ‘‘substitutes,’’
FSIS issued Policy Memo 123,
‘‘Modified Breakfast Sausage, Cooked
Sausage, and Fermented Sausage
Products Identified by a Nutrient
Content Claim and a Standardized or
Traditional Name,’’ and Policy Memo
121B ‘‘Labeling of Low Fat Ground Beef
and Low Fat Hamburger Containing
Added Ingredients,’’ in January of 1995.
These policy memoranda stated, among
other things, that these products are
permitted to be identified by a nutrient
content claim that reflects the reduction
in fat content in the product in
conjunction with the appropriate
standardized product name, e.g., ‘‘Fat
Free Bologna,’’ ‘‘Low Fat Pepperoni,’’ or
‘‘Low Fat Hamburger, Water, and
Carrageenan Product.’’ Both Policy
Memo 121B and Policy Memo 123 were
issued as interim measures until such
time that rulemaking could be
completed. Both of these policy
memoranda will be rescinded by this
final rule.
In this final rule, FSIS is establishing
a general definition and standard of
identity for modified versions of meat
and poultry products that substitute for
meat and poultry products defined by a
regulatory standard of identity or
composition in 9 CFR Part 319 and 381,
subpart P, i.e., ‘‘substitute standardized
products.’’ This rule is needed to
facilitate the development and
availability of substitute standardized
meat and poultry products that have
reductions in constituents that are of
health concern to some people, e.g., fat,
cholesterol, and sodium. The rule
allows FSIS to rely more on labeling
requirements and less on restrictive
recipe-type standards to carry out its
mandate to ensure that the labels of
meat and poultry products are truthful
and not misleading to consumers.
Comments and Agency Response
FSIS received 56 comments in
response to the proposed rule from
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members of the meat and poultry
processing industry, industry trade
associations, members of the flavoring
and ingredients industry, members of
the soybean industry, academia, health
professionals, governmental entities,
consumer advocacy groups, and
individual consultants. In general, the
comments submitted in response to the
proposed rule were favorable. Most
commenters agreed that FSIS should
establish a regulatory general standard
for substitute standardized products that
are lower in fat, cholesterol, or sodium.
One commenter opposed the rule
because the commenter believed it did
not go far enough in providing
flexibility to industry. This commenter
stated that, rather than converting FSIS
Policy Memo 123 into regulation, FSIS
should create a new standard for
substitute standardized meat and
poultry products to allow the use of
non-traditional ingredients in all
products, not just versions of products
that are identified by a nutrient content
claim and a standardized product name.
Response: FSIS recognizes the need to
explore this and other issues concerning
reform of the meat and poultry product
standards. However, expanding the use
of non-traditional ingredients for all
standardized products is an issue that is
outside the scope of this rulemaking.
The Agency is, however, exploring this
and other related issues in a separate
rulemaking to modernize meat and
poultry product standards. This
rulemaking is discussed in greater detail
later in this document.
Policy Memo 123 and Policy Memo
121B
Comment: A few commenters felt that
FSIS Policy Memo 121B and Policy
Memo 123 should remain in effect once
this final rule becomes effective so that
products produced under these policies
can continue to be manufactured. Other
commenters stated that the general
standard defined in the proposed rule
should apply to food products whose
standards are documented in the FSIS
Food Standards and Labeling Policy
Book (the Policy Book), as well as those
products whose standards of identity
and composition are codified in Parts
319 and 381, subpart P. The
commenters noted that the wording in
proposed 9 CFR 319.10(a) and
381.172(a) does not specifically include
the standards described in the Policy
Book, while FSIS Policy Memo 123
does. They were concerned that once
the rule is in place, and Policy Memo
123 is rescinded, certain products, such
as ‘‘Low Fat Pepperoni,’’ would no
longer be permitted because pepperoni
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does not have a standard of identity
codified in the regulations.
Response: The policy embodied in the
proposed general standard will also
apply to the informal standards for
products, such as pepperoni, that are
described in the Policy Book. Thus,
Policy Memo 121B and Policy Memo
123 will not remain in effect once the
proposed rule becomes final. FSIS
issued both Policy Memo 121B and
Policy 123 as interim measures to
accommodate certain lower fat
substitute meat and poultry products
until such time that rulemaking was
completed. This final rule incorporates,
expands, and codifies the intent of these
policy memoranda. Thus, rescinding
Policy Memo 121B and Policy Memo
123 will not preclude the production of
products that have been made under
those policies. The Agency intends to
clarify this point in a policy bulletin,
which is a more appropriate document
for addressing the informal standards
described in the Policy Book.
Nutrient Content Claims That
Emphasize the Presence of an
Ingredient
Comment: Some commenters
disagreed with the Agency’s proposal to
permit only expressed nutrient content
claims that relate to reductions in
constituents such as fat, cholesterol, or
sodium, in conjunction with the
standardized name of the substitute
product. These commenters felt that
nutrient content claims, such as ‘‘high
in’’ and ‘‘good source of,’’ that
emphasize the presence of an
ingredient, should also be permitted to
be used as part of the substitute
standardized product’s name, provided
that the product qualifies for these
claims under 9 CFR part 317 subpart B
or 9 CFR 381 subpart Y.
Response: Under the current
regulations, meat and poultry products
that satisfy the criteria for use of
nutrient content claims defined in 9
CFR part 317 subpart B and 9 CFR 381
subpart Y are permitted to make claims,
such as ‘‘high in’’ or ‘‘good source of,’’
that emphasize the presence of a
nutrient. The ability to make these kinds
of nutrient content claims is not affected
by this rulemaking.
In the preamble to the proposed rule,
FSIS noted that the meat and poultry
product standards did not appear to
preclude the making and marketing of
standardized products that qualify for
the use of claims such as ‘‘high in’’ and
‘‘good source of.’’ Therefore, in the
proposed regulation, the Agency did not
expressly provide for these types of
nutrient content claims in the general
standard. However, in the proposal,
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FSIS did solicit comments on whether
current regulatory standards prevent the
distribution of products with nutrient
content claims other than those that
reflect a reduction in the level of a
nutrient.
None of the comments received
suggested that the existing meat and
poultry product standards preclude the
making and marketing of standardized
products that qualify for the use of
claims such as ‘‘high in’’ or ‘‘good
source of.’’ Furthermore, because of the
FSIS policy that precludes direct
nutrient fortification of meat and
poultry products, standardized meat
and poultry products are not permitted
to be modified to qualify to use a
nutrient content claim by adding
nutrients to the product. Therefore, FSIS
has decided not to modify the scope of
coverage in this final rule to permit
nutrient content claims other than those
that reflect a reduction of constituents
that are of health concern to some
people, e.g., fat, cholesterol, and
sodium, to be used as part of the
product name. Products that qualify for
‘‘high in’’ and ‘‘good source of’’ nutrient
content claims may continue to
highlight these claims as provided in 9
CFR 317.354 and 9 CFR 381.454.
Nutrient Fortification
Comment: Four commenters
suggested that FSIS reexamine its policy
precluding direct nutrient fortification
of meat and poultry products. Two of
these commenters suggested that FSIS
allow selective nutrient fortification in
meat and poultry products to permit
standardized products to be modified so
that they qualify to use nutrient content
claims, such as ‘‘high in Vitamin A,’’ as
part of the product name. One of these
commenters requested that FSIS modify
the language in proposed 9 CFR
319.10(a) to delete the following
italicized words ‘‘* * * because of a
compositional deviation that results
from reduction of a constituent that is
described by an expressed nutrient
content claim * * *’’
Another commenter suggested that
FSIS permit selective protein
fortification in substitute standardize
products so that they may use claims
such as ‘‘High in Protein’’ and ‘‘Good
Source of Protein’’ as part of the product
name. This commenter recommended
that FSIS continue to require substitute
standardized products to meet the same
basic minimum meat and poultry
content requirements contained in the
existing meat and poultry product
standards, but that the overall protein
level in these products should be
allowed to be fortified using ingredients
such as soy protein. Another commenter
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33805
that expressed support for permitting
direct nutrient fortification of meat and
poultry products felt that, because the
over-consumption of protein in the
American diet, that protein fortification
should not be permitted.
Two other commenters requested that
FSIS allow fortification to replace
vitamins and minerals that may be lost
due to formulation adjustments to
produce nutrient-modified foods. These
commenters also requested that FSIS
exempt substitute standardized
products subject to the general standard
from the minimum meat and poultry
content requirements imposed by the
existing meat and poultry product
standards. Both commenters suggested
that for these substitute products, FSIS
should focus on nutritional equivalency
to the traditional standardized product
rather than meat content equivalency,
and permit reductions in the meat and
poultry content for purposes of reducing
the product’s fat content. The
commenters stated that if FSIS were to
permit such reductions in the meat and
poultry content, fortification might be
necessary to replace lost nutrients.
One commenter suggested that, while
existing FDA regulations state that the
FDA does not consider it appropriate to
fortify meat and poultry products (21
CFR 104.20(a)), the FDA regulations
appear to make an exception for
fortification of foods that replace
traditional foods when fortification is
necessary to avoid nutritional
inferiority.
Response: The comments requesting
that FSIS reexamine its policy on
nutrient fortification raise some
interesting points, particularly with
respect to the issues concerning
nutritional equivalency versus meat
content equivalency. However, the
decision to allow fortification of meat
and poultry products involves several
complex issues, many of which are
outside the scope of this rulemaking.
FSIS’’ fortification policy is derived
from FDA’s policy statement on nutrient
fortification codified at 21 CFR part 104,
subpart B, which states, in part, that the
FDA ‘‘* * * does not consider it
appropriate to fortify fresh produce;
meat, poultry, or fish products * * *
(21 CFR 104.20(a)). The fundamental
objective of FDA’s fortification policy is
‘‘* * * to establish a uniform set of
principles that will serve as a model for
the rational addition of nutrients to
food’(21 CFR 104.20(a)). As stated in its
policy, FDA determined that, ‘‘* * *
random fortification of foods could
result in over-or under-fortification in
consumer diets and create nutrient
imbalances in the food supply’’ (21 CFR
104.20(a)).
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FSIS has a long history of prohibiting
direct fortification of meat and poultry
products, which is supported by the
codified FDA fortification policy. Thus,
when determining whether to revise its
nutrient fortification policy for meat and
poultry products, FSIS must consider
the issues in relationship to the codified
FDA policy statement on fortification.
Furthermore, in order to maintain
consistent policies regarding nutrient
fortification between the two agencies,
any effort by FSIS to revise its
prohibition on direct nutrient
fortification of meat and poultry
products should include FDA
participation and involve the scientific
community (e.g., the National Academy
of Sciences, Institute of Medicine). FSIS,
FDA, and the scientific community need
to first consider the guiding scientific
principles that form the basis for
establishing a public health need for
fortifying meat and poultry with
nutrients. Only after these principles are
applied could there be consideration of
revising the current fortification policy.1
Obviously, this type of effort is outside
the intended purpose and scope of this
rulemaking. It would be more
appropriate to consider this matter in a
separate rulemaking where the Agency
can receive the benefit of an open and
thorough review of all issues related to
the fortification of meat and poultry
products.
Furthermore, FSIS believes that the
formulation adjustments needed to
produce substitute standardized
products with reductions in
constituents such as fat, cholesterol, and
sodium, will not result in a product that
is nutritionally inferior to the product
for which it is a substitute. Important
nutrients, such as iron, zinc, B vitamins,
and protein, are associated with the lean
muscle portion of meat and poultry
tissue, not the fat. Because the
minimum meat and poultry requirement
for substitute standardized products is
not changed by this rule, reductions in
the fat content should not affect the
levels of nutrients associated with the
lean muscle portion of these products.
Therefore, nutrient fortification is not
necessary to prevent the products
subject to the general standard defined
by this rule from being nutritionally
inferior to the standardized products for
which they are a substitute.
1 See report: Institute of Medicine, National
Academy of Science, 2003. Dietary Reference
Intakes, Guiding Principles for Nutrition Labeling
and Fortification. The National Academies Press,
Washington, DC.
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Differences in Performance
Characteristics
Comment: The proposed regulation
stated that a substitute standardized
product with performance
characteristics, e.g., cooking quality,
freezing quality, spreadability of
product, and shelf-life, that materially
limit the use of the product must
include a disclaimer on the product’s
label adjacent to the product name
informing the consumer of such
differences.
Most commenters agreed that
limitations in a product’s performance
characteristics should be disclosed on
the product label, and be conspicuous
and readable. A number of commenters
stated that the disclaimer should be
adjacent to the most prominent claim on
the label. One commenter, although in
agreement with the disclaimer
requirement, felt that disclosure on the
label, not necessarily adjacent to the
product name as provided in the
proposed rule, was sufficient to inform
the consumer of performance
differences. This same commenter
recommended that FSIS harmonize the
requirement for labeling of performance
differences with a similar FDA rule,
which requires a disclaimer adjacent to
the most prominent claim on the label
(21 CFR, 101.13(d)). Another commenter
stated that the disclaimer should be
adjacent to the most prominent claim
and should most likely appear on the
principal display panel.
Response: In the preamble to the
proposed rule, FSIS stated that ‘‘if there
is a difference in performance
characteristics that materially limits the
use of the product, the product may still
be considered a substitute if the label
includes a disclaimer adjacent to the
most prominent claim in accordance
with 9 CFR 317.313(d)(1) and (2) and 9
CFR 381.413(d)(1) and (2), informing the
consumer of such difference’’ (60 FR
67480). However, in the text of the
proposed rule, FSIS stated that the label
must include, ‘‘adjacent to the product
name,’’ a statement in accordance with
9 CFR 317.313(d)(1) and (2) and 9 CFR
381.413(d)(1) and (2) informing the
consumer of differences in performance
characteristics (60 FR 67486, 67487).
Thus, the preamble and the text of the
proposed rule differed in that the
preamble did not mention that the
disclaimer must be ‘‘adjacent to the
product name.’’ The regulations
referenced by both the preamble and the
text of the proposed rule, 9 CFR
317.313(d)(1) and 9 CFR 381.413(d)(1),
require that differences in performance
characteristics that materially limit the
performance of a substitute product be
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disclosed adjacent to the most
prominent claim on the product label.
FSIS is resolving the discrepancy
regarding placement of the disclaimer.
FSIS agrees with the comment that
disclosure on the label, not necessarily
adjacent to the product name, is
sufficient to inform the consumer of
performance differences. Therefore, in
this final rule, FSIS is not requiring that
the disclaimer be placed adjacent to the
product name. As in FDA regulations 21
CFR 130.10 and 101.13(d), a disclaimer
for differences in performance
characteristics shall be placed adjacent
to the most prominent claim on the
label. To reflect this decision, FSIS is
removing the phrase ‘‘adjacent to the
product name’’ from proposed
§§ 319.10(b)and 381.172(b).
Comment: Two commenters disagreed
with the need for the proposed
disclaimer requirement and suggested
that disclosure of any limitations in the
performance characteristics of a
substitute standardized product be
voluntary. One of these commenters
stated that disclaimers on a product’s
labeling informing consumers of
performance characteristics that
materially limit the use of the product
need not be required by regulations
because a substitute standardized
product produced under the general
standard will succeed or fail in the
market place based on consumer
expectations associated with the
product’s performance. This commenter
stated that businesses would voluntarily
place disclaimers on a product’s label in
the absence of a regulation requiring
that they do so because it would be good
business to inform consumers that a
product they are purchasing can not be
used in a traditional application.
The other commenter agreed that, in
practice, poorly formulated products
would fail in the marketplace long
before any regulatory system could
determine that they did not meet the
specific performance characteristics
they would be expected to have.
However, this commenter
acknowledged that requiring a
disclaimer informing consumers of
limitations in a product’s performance
characteristics, when they exist, will
require manufacturers of substitute
standardized products to monitor
performance characteristics during
product development and may help
ensure that new low- and reduced-fat
standardized products are formulated
well from the beginning. The
commenter went on to state that
consumers are also more likely to accept
this category of substitute products if
they are well formulated from the
beginning.
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Response: FSIS disagrees with the
commenters’ suggestion that disclosure
of performance characteristics that
materially limit the use of a substitute
standardized product compared to the
use of the traditional standardized
product should be voluntary. The FMIA
and the PPIA require that the labeling of
a meat or poultry product must be
truthful and not misleading, and that
such labeling accurately disclose to
consumers what they are buying when
they purchase any meat or poultry
product. Information disclosing
differences in performance
characteristics that affect the use of a
substitute standardized product (e.g.,
cooking quality, freezing quality,
spreadability of product, and shelf life)
is a material fact that must be disclosed
on the labeling of these products.
Without such labeling, consumers
would be misled about significant
characteristics and uses the product has
compared to the standardized product
for which it substitutes. Accordingly,
this information must be communicated
to consumers on the product’s label, or
the label will be misleading and the
product will be misbranded under the
FMIA or PPIA.
Moreover, FSIS agrees with the
commenter who suggested that
processors are more likely to monitor
the performance characteristics of
substitute standardized products during
product development when limitations
in the product’s performance
characteristics are required to be
disclosed on the product’s labeling.
FSIS also agrees that if substitute
standardized products are well
formulated from the beginning, it will
promote consumer acceptance of this
category of meat and poultry products.
Comment: One commenter pointed
out that it may be possible for
performance characteristics to be
introduced into a substitute
standardized product that improve upon
the performance characteristics of the
traditional standardized product. The
commenter suggested that the Agency
consider substituting the term ‘‘not
inferior’’ for ‘‘similar’’ in proposed 9
CFR 319.10(b).
Response: FSIS did not intend to
prohibit improvements in the
performance characteristics of substitute
products when it proposed that
substitute standardized products subject
to the general standard perform
similarly to the traditional standardized
products for which they substitute.
However, FSIS disagrees that it should
require that substitute standardized
products have performance
characteristics that are ‘‘not inferior to’’
rather than ‘‘similar to’’ the traditional
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standardized products as suggested by
the commenter. As proposed,
§§ 319.10(b) and 381.172(b) permit
products subject to the general standard
to have limitations in performance
characteristics provided that such
limitations are properly disclosed on the
product’s labeling. The Agency believes
that requiring disclosure of any
performance limitations on the labeling
of products subject to the general
standard provides sufficient incentive
for manufacturers of these products to
market products that are not inferior to
the traditional standardized products.
Furthermore, proposed 9 CFR 319.10(b)
and 9 CFR 381.172(b) require a
disclaimer for performance
characteristics that ‘‘materially limit’’
the use of a substitute standardized
product, not for characteristics that
improve the performance of the product.
Thus, the disclaimer requirement
contained in proposed 9 CFR 319.10(b)
and 9 CFR 381.172(b) will not
discourage manufacturers from making
improvements to the performance
characteristics of substitute products
when it is possible to do so.
Enforcement
Comment: Two commenters
questioned FSIS’s ability to enforce and
ensure uniform compliance with the
performance characteristics
requirements proposed in 9 CFR
319.10(b) and 381.172(b). One
commenter asked how FSIS intends to
determine differences in performance
characteristics. The commenter went on
to state that the proposed performance
characteristics requirements seem to be
‘‘command and control’’ regulations that
are not related to product safety. The
other commenter stated that, in practice,
poorly formulated products would fail
in the marketplace long before any
regulatory system could determine that
they did not meet the specific
performance characteristics discussed in
the proposal.
Response: FSIS expects that substitute
standardized products that are produced
under the general standard will conform
to the performance characteristics
requirements set forth in proposed 9
CFR 319.10(b) and 381.172(b). To
ensure that there is compliance, FSIS
will examine the performance
characteristics and product quality of
substitute products as it would other
types of products, through scientific
review and experimental investigations.
In addition, FSIS will use traditional
methods available to the Agency, such
as sample analysis, inspections, surveys,
and follow-up investigations of
consumer and trade complaints to
identify products that do not comply
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with the new regulations in order to
enforce this regulation as the need
arises.
Furthermore, FSIS disagrees with the
comment that the proposed performance
characteristics requirements are
‘‘command and control’’ regulations.
Under §§ 319.10(b) and 381.172(b), FSIS
is not establishing specific criteria for
determining similarities in performance
characteristics. FSIS believes that
judgments about similarity are best left
to product developers, who have the
incentive to market a product that
resembles the traditional standardized
product as closely as possible and to
disclose product performance
limitations to ensure that there is
consumer satisfaction with the
substitute standardized product.
Safe and Suitable Ingredients
Comment: There was general
agreement among the commenters that
the ingredients used in a substitute
standardized product produced under
the general standard should be those
ingredients provided by the traditional
standard, with the exception of ‘‘safe
and suitable ingredients,’’ as defined in
(former) 9 CFR 318.7 and 381.147, at the
minimum level necessary to improve
texture and prevent syneresis. However,
several commenters requested
clarification and expansion of the
ingredients permitted under this
provision.
Three commenters stated that
allowances for ingredients should be
broadened to include any safe and
suitable ingredients to replace
functional characteristics. These
commenters all noted that the FSIS
proposal limits ingredient usage to
achieve textural improvement and to
prevent syneresis. They felt that FSIS
should build additional flexibility into
the final rule to allow for a wider use
of safe and suitable ingredients to
replace functional characteristics that
may be lost when a formulation is
adjusted to meet a claim requirement.
These commenters mentioned that the
comparable FDA regulation allows the
use of safe and suitable ingredients
‘‘* * * to add flavor, extend shelf life,
improve appearance, or add sweetness’’
(21 CFR 130.10(d)). One commenter
suggested that any ingredient that is
generally recognized as safe (GRAS) or
that is an approved additive should be
permitted to be used as desired by the
manufacturer. Another commenter
stated that limiting the use of safe and
suitable ingredients to the minimum
level necessary to improve texture and
to prevent syneresis severely limits the
ability to produce a consumeracceptable meat or poultry product. One
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commenter specifically requested that
FSIS clarify the acceptability of
flavorings, especially meat flavorings, as
safe and suitable ingredients in
substitute standardized products.
Response: For purposes of
clarification, since it published the
general standard proposal, FSIS issued
the final rule ‘‘Food Ingredients and
Sources of Radiation Listed or
Approved for Use in Meat and Poultry
Products’’ (64 FR 72168, December 23,
1999). The rule is intended to improve
the efficiency of the procedures used by
FSIS and FDA to review and approve
the use of food ingredients and sources
of radiation in the production of meat
and poultry products. Under the new
regulations, rather than listing
substances approved for use in the
production of meat and poultry
products in the chart of substances
contained in former 9 CFR 318.7(c)(4)
and former 9 CFR 381.147(f)(4), FDA
now lists food ingredients and sources
of radiation that are safe for specific use
in the production of meat and poultry
products in its regulations in title 21 of
the CFR. In the final rule, FSIS also
created a list of food ingredients
approved for use in the production of
meat and poultry products by
combining the listing contained in
former section 318.7(c)(4) with the
listing contained in former section
381.147(f)(4) and moving the combined
listing to section 424.21(c). The final
rule became effective on January 24,
2000.
FSIS did not include ingredients that
would affect flavor, shelf life, or
sweetness because these kinds of
ingredients do not affect the ability of a
manufacturer to modify a meat or
poultry product to reduce fat,
cholesterol, or sodium, which was the
focus of this rulemaking. Thus,
§§ 319.10 and 381.172 provide only for
increased amounts of safe and suitable
ingredients that are needed to achieve
the effect of replacing fat, i.e., binders,
texturizers, and emulsifiers.
As for the acceptability of flavorings
in substitute standardized products,
manufacturers will not be limited by
§§ 319.10 or 381.172 in their ability to
use ingredients that impart flavor. This
final rule does not limit a
manufacturer’s ability to use safe and
suitable meat and poultry flavorings.
‘‘Fat Replacing’’ Binders
Comment: In the preamble to the
proposed rule, FSIS provided a list of
‘‘fat replacing’’ binders to assist meat
and poultry processors to understand
the types of ingredients that are
permitted to be used to achieve the
effects of fat in making substitute
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standardized products under the general
standard. However, the list was not
intended to be all-inclusive. One
commenter supported the use of
ingredients not identified in the
preamble as part of a fat replacement
system and requested that FSIS clarify
whether other fat replacers, such as milk
protein concentrates, would be
permitted in substitute standardized
products, given this substance’s
similarities to the listed substances. The
commenter also requested that the
preamble to the final rule specifically
note that milk protein concentrates and
egg whites are acceptable substances in
fat replacement systems.
Three commenters agreed that the
ingredients listed in the preamble are
appropriate for use in a substitute
version of a standardized product but
felt that the list should be broadened to
include other safe and suitable
ingredients that have a demonstrated
ability to function as a fat replacement
system. One of these commenters
requested that if the list provided within
the context of the preamble is not meant
to be all-inclusive, FSIS should state
that fact. The commenters also
encouraged FSIS to include a list of
criteria for evaluating fat replacing
binders not on the list to determine
whether they qualify as acceptable
binders.
Response: The list of ‘‘fat-replacing
binders’’ presented in the preamble to
the proposed rule represents examples
of ingredients or additives historically
classified as binders by food scientists
and ingredient technologists. This list is
not intended to be all encompassing,
and other safe and suitable ingredients
historically recognized as binders are
permitted to be used in ‘‘fat
replacement’’ systems for substitute
standardized products produced under
the general standard.
In general, a safe and suitable
ingredient qualifies for use as a fat
replacing binder under this final rule if
it is only used for its functional
properties and does not impart other
characterizing qualities, such as taste
and nutritional value, to the
standardized product when used in the
product formulation. FSIS will evaluate
whether safe and suitable ingredients
that were not listed in the preamble to
the proposal qualify as fat replacing
ingredients on a case-by-case basis.
As a point of clarification, milk
protein concentrates have historically
been used by meat and poultry product
manufacturers as binding ingredients in
meat and poultry products and
therefore, under the general standard,
FSIS will permit milk protein
concentrates to be used as binders in fat
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replacement systems for substitute
standardized products.
Regarding the use of egg whites as a
fat replacing binder, egg whites are
considered an egg product and as such
function as an individual food product
that is consumed for its own taste and
nutritional value. Thus, FSIS considers
the use of egg whites in the formulation
of a meat or poultry product to be
sufficiently characterizing so as to result
in a product that is not a substitute
standardized product, but one that is a
non-standardized product, e.g.,
identified with a true product name,
such as ‘‘Low Fat Pork Sausage made
with Egg Whites.’’
Although FSIS is not providing an all
inclusive list of suitable fat replacing
binders in this final rule, the Agency
did provide an extensive listing of
binders in the preamble to the proposed
rule to convey the intent of the rule (see
60 FR 67481). Persons interested in
determining whether an ingredient is an
appropriate fat replacing binder may
refer to this original listing.Furthermore,
safe and suitable ingredients that meet
the general criteria outlined above, i.e.,
have historically been classified as
binders, are only used for their
functional properties, and do not impart
other characterizing qualities when used
in the formulation of substitute
products, will also qualify as acceptable
fat replacing binders under this final
rule.
Textured Vegetable Protein (TVP) as a
‘‘Fat Replacer’’
Comment: In the preamble to the
proposed rule, FSIS stated that the
Agency views TVP as a ‘‘meat or poultry
replacer,’’ and that the use of TVP as a
fat replacing ingredient in a substitute
standardized product subject to the
general standard would be
inappropriate. At the time that the
proposal was published, FSIS had
determined that the use of TVP in a
substitute standardized product would
change the nature of the product to such
an extent that it would no longer be a
substitute product within the
parameters of the proposed rule. This
view, in part, was based on the belief
that TVP was used as a ‘‘meat
replacing’’ ingredient in foods
considered ‘‘meat replacing products,’’
such as ‘‘veggie-burgers,’’ which are
primarily TVP with water, flavorings,
and seasonings.
FSIS received numerous comments
expressing strong disagreement with
FSIS’s historic views. Forty-three
commenters submitted statements in
support of allowing TVP as a fat
replacer in substitute standardized meat
and poultry products subject to the
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general standard so that these products
may be identified by a nutrient content
claim. Many of these commenters
provided supporting studies on the
health and nutritional benefits of soy
protein, along with data on consumer
awareness and acceptance of products
containing TVP. Many commenters felt
that not permitting TVP as a fat
replacing ingredient would greatly limit
the ability of the industry to develop
substitute standardized meat and
poultry products that are lower in fat.
These commenters stated that the use of
TVP as a fat replacer is important in
expanding the flexibility of the meat
and poultry industry to create and
market an increased variety of healthful
substitute meat and poultry products.
Some commenters specifically
mentioned that prohibiting TVP would
limit product development in areas of
coarse ground cooked and fermented
sausage.
Several commenters stated that TVP
should be permitted as a fat replacer so
long as its use conforms to the
requirements of the general standard.
These commenters stated that TVP
should be permitted as part of a ‘‘fat
replacement system’’ in substitute
standardized meat and poultry products
so long as: (1) Its use does not
substantially change the nature of the
finished product; (2) it is not used to
replace the meat or poultry content
required by the traditional standard; and
(3) it is used only at the minimum level
necessary in a fat replacement system to
qualify for use of the nutrient content
claim.
A number of commenters stated that
TVP should be regulated on the basis of
its functional properties rather than on
its physical form. Many of these
commenters pointed out that, while in
the past TVP was used as a ‘‘filler’’ or
‘‘substitute’’ for meat components in
food, advancements in TVP technology
have made TVP a highly functional
ingredient that could now be used as
part of a fat replacement system to
improve the textural character and
quality of a substitute standardized meat
or poultry product. Many commenters
noted that TVP, when used in
combination with other water binders,
provides improved product texture,
visual appearance, performance, and
storage characteristics. Data supporting
this view were presented to the Agency.
Some commenters felt that TVP
should be allowed as a fat replacer in all
meat items where non-textured
vegetable proteins are allowed. One
commenter stated that texture is a
matter of degree, and that forms of
vegetable proteins range from fine
powders, to small granules, to small
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flakes, to larger granules and flakes.
This commenter stated that it is
arbitrary to require that TVP be
excluded as a ‘‘fat replacer’’ but not the
powdered forms. One commenter
questioned the logic of permitting soy
flour, soy protein concentrate, and
isolated soy protein in products because
they replace fat, but prohibiting the use
of TVP because it is inappropriately
thought to replace meat. The commenter
pointed out that the proposed rule does
not permit a reduction in the meat or
poultry content, and therefore, TVP
could not be used as a meat replacer.
Another commenter mentioned that
other binders, such as carrageenan, can
be texturized, and therefore, TVP is
being singled out unfairly.
A number of commenters stated that,
because the presence of TVP can be
disclosed in product labeling,
consumers should be allowed to decide
for themselves whether to purchase a
lower fat standardized product that
contains TVP. Some commenters
pointed out that the presence of TVP in
a meat food product could be
communicated to consumers in the
same manner as any other ingredient, in
the ingredient statement. The
commenters asserted that appropriate
product labeling required by the general
standard would ensure that consumers
would not be misled about the presence
of TVP in substitute standardized
products produced.
Some commenters stated that if TVP
is permitted as a fat replacer in
substitute standardized products, the
substitute product should provide the
same amount of animal protein as the
traditional standardized product. One
commenter stated that this approach
would provide manufacturers with
optimum flexibility, yet guarantees that
the consumer receives a product that is
at least as valuable as the unmodified
product. Another commenter mentioned
that consumers are interested in over-all
nutrition, not in specific ingredients.
Some commenters expressed the view
that TVP should not be considered as a
‘‘food,’’ because it is not consumed by
itself as a food. These commenters
stated that TVP is a functional food
ingredient that can be used as part of a
fat replacement system.
Response: FSIS has been persuaded
by the comments, information, and
other data submitted by commenters to
permit the use of TVP as a part of a fat
replacing system in substitute
standardize products produced under
the general standard. Accordingly, in
this final rule, proposed §§ 319.10(c)
and 381.172(c) have been modified to
provide for the use of TVP, alone or in
combination with other binders and
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water, as part of a fat replacement
system.
The Agency will permit the use of
TVP as a functional food ingredient that
is used to replace fat. Like the other fat
replacing ingredients permitted to be
used under this final rule, the use of
TVP as an ingredient in a substitute
standardized product will be permitted
only at the lowest level necessary to
achieve the intended effect of replacing
fat. When TVP is used to replace fat, the
ingredients statement on the product
label must alert the consumer to the fact
that TVP is not permitted in the
traditional standardized product or is
used in excess of amounts permitted in
the traditional standardized product.
The labeling requirements will ensure
that consumers will not be misled when
TVP is used to replace fat in substitute
standardized meat and poultry products
subject to the general standard.
Under this final rule, TVP may not be
used to replace the meat or poultry
content of a product when a product
standard specifies a minimum meat or
poultry content requirement. However,
if the formulation of a substitute
product produced under the general
standard contains the same amount of
meat or poultry prescribed by the
traditional standard, the fat component
of the meat or poultry in the substitute
product may be removed during
processing and replaced with TVP, or
any other safe and suitable binder, alone
or in combination with water as part of
a fat replacement system.
For example, the product standard for
‘‘chili con carne’’ provides that the
product shall contain not less than 40%
meat computed on the weight of the
fresh meat (9 CFR 319.300). The product
formulation for a substitute version of
chili con carne produced under the
general standard must contain 40%
meat, but the fat content of the meat
component may be replaced with TVP
during processing.
According to information presented to
the Agency, TVP is particularly useful
in developing lower fat versions of
cooked sausages and other comminuted
meat and poultry products. Although
the standards for these kinds of
products generally do not prescribe a
minimum meat or poultry content, most
of these standards limit the amount of
fat that is permitted in the product. For
example, the standard for cooked
sausages defined in 9 CFR 319.180
limits the fat content of these products
to no more than 30% of the finished
product, and the standard for ground
beef defined in 9 CFR 319.15 limits the
fat content in this product to no more
than 30%. Thus, under this final rule,
the amount of TVP permitted in such
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products will be limited by both the
requirement that fat replacing
ingredients may be used only at the
lowest level necessary to replace fat and
by the minimum fat content
requirement established by the product
standard.
For example, a substitute cooked
sausage produced under the general
standard is permitted to contain up to
30% TVP, provided that the sole
function of the TVP is to replace the fat.
For purposes of this rule, FSIS does not
consider replacing the fat component of
a single ingredient standardized
product, such as ground beef, as
reducing the product’s meat content,
provided that the product complies with
the manufacturing and labeling
requirements prescribed in this final
rule.
To eliminate the possibility of
confusion, the phrases ‘‘textured
vegetable protein shall not replace
meat’’ and ‘‘textured vegetable protein
shall not replace poultry,’’ which were
used as examples in the regulatory text
of proposed 9 CFR 319.10(c)(2) and
381.172(c)(2), will be removed in the
final rule. These phrases are
unnecessary because the regulation
already prohibits reductions in the meat
or poultry content required by a
regulatory standard regardless of
whether TVP is used in the product.
Other Foods as ‘‘Fat Replacers’’
Nine commenters indicated that in
the final rule, FSIS should permit foods,
such as bread, rice, potatoes, fruits, and
vegetables to be used in substitute
standardized meat and poultry products
to reduce their fat content. Some of
these commenters stated that these
ingredients could serve the same role as
the water and binder systems permitted
as fat replacers in the proposed rule, but
that food ingredients are more beneficial
because they may contain some
nutritional constituents, such as
vitamins and minerals, that many
binders do not. One commenter stated
that food ingredients, when used at
proper levels, help to provide
consumers with substitute standardized
products that perform similarly to
traditional standardized products.
Another commenter stated that the
nutrition label would enable consumers
to make informed purchase decisions
based on the entire nutritional profile of
the product. This commenter pointed
out that many consumers would prefer
the nutritional profile of substitute
standardized products that use starchy
vegetables and complex carbohydrates,
such as rice and potatoes, rather than a
combination of water and ingredients
such as highly refined vegetable gums to
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lower the percentage of calories from
fat. One commenter stated that it makes
sense to allow other foods as fat
replacers if the goal is to make more
healthful products available to
consumers. Another commenter
suggested that consumers might be more
interested in overall nutritional quality,
taste, convenience, and performance of
the product than in the specific
ingredients present in the product.
Response: FSIS concedes that because
foods such as bread, rice, potatoes,
fruits, and vegetables, have little or no
fat, their use as ingredients in
standardized meat and poultry product
could have the effect of reducing the fat
content of such products. However,
when foods are used as ingredients in a
standardized product, the composition
of the product may be altered to such an
extent that the resulting product is not
a substitute version of the traditional
standardized product but a new and
different product with a separate
identity that reflects the combination of
the individual foods. For example,
because diced apples and rice are not
specified as ingredients in the
standardized product ‘‘Pork Sausage,’’
when they are added to ‘‘Pork Sausage,’’
the result is a new product, which,
provided that it does not have a
standard of identity or composition
prescribed by 9 CFR part 319 or other
established common or usual name, is
required to bear a descriptive name,
such as ‘‘Pork Sausage with Diced
Apples and Rice,’’ that clearly identifies
the product (see 9 CFR 317.2(c)(1) and
(e) and 9 CFR 381.117(a)). Because the
product ‘‘Pork Sausage with Diced
Apples and Rice’’ is a new product and
not a substitute version of the
standardized product ‘‘Pork Sausage,’’ it
is not the type of product that the
general standard established by this
final rule is intended to address.
As a point of clarification, this final
rule does not prevent non-standardized
meat and poultry products that use food
ingredients to reduce their fat content
from using a traditional nutrient content
claim permitted under 9 CFR 317
subpart B and 381 subpart Y, provided
they meet the requirements of the claim.
For example, the product ‘‘Pork Sausage
with Diced Apples and Rice’’ is
permitted to bear the claim ‘‘low fat’’ on
its label if it complies with § 317.362,
and therefore, may be referred to as
‘‘Low Fat Pork Sausage with Diced
Apples and Rice.’’ Consumers who
prefer the nutritional profile of meat and
poultry products that use other foods,
rather than binders and water, or other
functional food additives, to reduce
their fat content will be able to identify
these products by their descriptive
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product name and the traditional
nutrient content claim on the product
labeling. Furthermore, any benefits in
the nutritional profile of products that
use foods as ingredients to reduce their
fat content will be reflected in the
nutrition facts panel, as well, if
appropriate, in other nutrient content
claims.
Prohibited Ingredients
Comment: One commenter expressed
agreement with the provision in
proposed 9 CFR 319.10(c)(3) and
381.172(c)(3) that states that ingredients
specifically prohibited for use in
standardized meat and poultry products
should also be prohibited for use in
substitute standardized products subject
to the general standard. However, the
commenter felt that ingredients
prohibited from use in all meat and
poultry products should be based on
safety considerations rather than quality
considerations.
Response: The general standard
allows for the use of any safe and
suitable fat replacement ingredient, e.g.,
binders and water. Under the Federal
Food, Drug, and Cosmetic Act (21 U.S.C.
301 et seq.), FDA is responsible for
determining the safety of food
ingredients for use in food in general.
Under the authority of the FMIA and
PPIA, FSIS acquiesces to FDA’s safety
judgments, but FSIS determines the
suitability of ingredients determined to
be safe by FDA for use in meat and
poultry products. These responsibilities
are fully described in the final rule
‘‘Food Ingredient and Sources of
Radiation Listed or Approved for Use in
the Production of Meat and Poultry
Products,’’ which was published in the
December 23, 1999, Federal Register (64
FR 72168).
Thus, although it is the responsibility
of the FDA to evaluate the safety of a
substance for use in meat or poultry
products, under the authority of the
FMIA and PPIA, FSIS may preclude the
use of a substance in meat or poultry
products for reasons other than safety.
There are instances in which the use of
a substance, even if safe, may promote
deception when used in a meat and
poultry product, and, accordingly, such
use would be prohibited by FSIS. For
example, paprika is considered GRAS
by FDA and is also listed for use as a
color additive, but the FSIS regulations
prohibit its use on fresh, uncooked meat
products because such use adds color
that may make the meat appear fresher
than it actually is (9 CFR 424.23(a)(1)).
Therefore, it is incumbent upon FSIS to
consider suitability, as well as the
safety, of ingredients for use in the
production of meat and poultry
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products in order to prevent these
products from being adulterated or
misbranded.
Processing Methods/Anatomical
Location for Meat and Poultry
Ingredients
Comment: One commenter stated that
the provision in proposed §§ 319.10 and
381.172 that requires that the meat
portion of a substitute standardized
product undergo the same basic
processing procedures as the traditional
standardized product for which it is a
substitute has the potential to limit the
use of new technologies without
producing any stated goal that would
justify the limitation. The commenter
stated, that as long as the substitute
standardized product has performance
characteristics that are similar to the
traditional standardized product, and is
produced only from authorized
ingredients, additional restrictions on
processing procedures are unnecessary
and undesirable.
Another commenter stated that the
general standard should permit
substitute standardized products to
contain different meat species and
different kinds of poultry than those
prescribed by the traditional standard,
and that it should permit meat or
poultry from different anatomical
locations than the locations prescribed
by the traditional standard, provided
that the difference in species or
anatomical location is stated in the
product name. This commenter felt that
a literal reading of the proposed
regulation could be interpreted to mean
that products such as ‘‘Beef Bacon’’ or
‘‘Pork Shoulder Bacon’’ would no longer
be permitted to include the term
‘‘Bacon’’ in their product names if
coupled with a nutrient content claim.
The commenter went on to say that
these kinds of products should continue
to be permitted to be marketed under
the same familiar names that have been
used in the past, and that use of a
nutrient content claim next to the
product name should not change this.
Response: The intent of the general
standard for substitute standardized
products is to enable the meat and
poultry industries to produce modified
versions of standardized products that
have reductions of certain constituents
that are of health concern to some
consumers, such as fat, cholesterol, and
sodium, and to increase flexibility and
support product innovation. Under this
rule, deviations from the existing
standards are not expected to result in
a product that no longer resembles the
original standardized product. Thus, the
use of a different meat species or kind
of poultry, or the use of meat or poultry
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from different anatomic locations from
those specified in the standard, that
results in a product that is so physically
dissimilar from the traditional
standardized product that it does not
meet the definition of ‘‘substitute’’ set
forth in 9 CFR 317.313(d) and
381.413(d) would be inconsistent with
the intent of this rule. For these kinds
of products to represent themselves as
substitute standardized products would
be false and misleading under the FMIA
and PPIA.
As an illustration, the regulatory
standard for ‘‘Bacon’’ under 9 CFR
319.107 requires that this product be
prepared from cured, sliced pork bellies.
Curing and slicing a cut of meat from a
different livestock species or from a
different anatomical location, or
preparing sliced pork bellies using a
method other than curing, would result
in a product with physical
characteristics so different from the
standardized product ‘‘Bacon’’ that the
resulting product could not be
considered a ‘‘substitute’’ for bacon
under 9 CFR 317.313(d) and 381.413(d).
Thus, instead of being identified as a
substitute product, the product would
be identified by a descriptive term such
as ‘‘Beef Bacon’’ or ‘‘Pork Shoulder
Bacon.’’
However, FSIS will consider the types
of changes requested by the
commenters, such as amending a
standard to permit the use of alternative
processing methods, on a case-by-case
basis. FSIS agrees that certain
technologies used to prepare
standardized foods may yield a product
with the same physical, nutritional, and
sensory characteristics as the food made
in accordance with the traditional
standards. To reflect this fact, instead of
specifying that substitute standardized
products must contain all ingredients
specifically required by a standard of
identity or composition, and that the
meat or poultry portion of substitute
products come from the same
anatomical location, be of the same kind
and amount, and undergo the same
basic processing procedures as the
standardized product as was proposed,
FSIS is revising §§ 319.10(c)(4) and
381.172(c)(4) to require only that
substitute standardized products
comply with all other applicable
standards of identity or composition.
Regarding the comment expressing
concern that under the general standard,
products such as ‘‘Beef Bacon’’ or ‘‘Pork
Shoulder Bacon’’ would no longer be
permitted to include ‘‘Bacon’’ in their
product names if coupled with a
nutrient content claim, as previously
mentioned, FSIS intends to apply the
principles embodied in the general
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standard established by this final rule to
other products as appropriate. The
Agency will clarify this fact in a policy
bulletin after this final rule is published.
Thus, this final regulation will not
prohibit the ‘‘bacon-like’’ products
described in the Policy Book, such as
‘‘Turkey Bacon-Cured Turkey Breast
Meat-Chopped and Formed,’’ from being
modified to qualify to use a nutrient
content claim as part of the product
name. The modified version of this
‘‘bacon-like’’ product would be
permitted to be identified as ‘‘Low Fat
Turkey Bacon-Cured Turkey Breast
Meat-Chopped and Formed.’’ FSIS
reiterates that the intent of this rule is
to provide a wider array of nutritionally
improved substitute products that
would provide consumers with more
meat and poultry products from which
to choose. The intent is not to diminish
or interfere with markets providing
innovative as well as traditional kinds
of products to consumers.
Minimum Meat and Poultry
Requirement
Comment: Several commenters
submitted statements both for and
against the proposed requirement that a
substitute standardized product subject
to the general standard rule maintain
the same minimum meat or poultry
requirement as the standardized product
for which it is a substitute. Seven
commenters agreed that substitute
standardized products should be
required to maintain the minimum meat
and poultry requirement established by
the traditional standard, while ten
commenters expressed disagreement
with this requirement.
Several commenters stated that the
meat or poultry content of a
standardized product often contains the
highest concentration of fat, and, while
it may be theoretically possible for
manufacturers to use leaner meat to
reduce fat, it is not economical. One of
these commenters stated that fatreduced products that meet the existing
minimum meat or poultry content
requirement would be prohibitively
expensive. Another commenter stated
that relying exclusively on leaner meat
to reduce fat might also make products
tougher in texture and less palatable.
Another commenter stated that, without
reducing the ‘‘meat block’’ (meat or
poultry content), the proposed general
standard can not deliver on its promise
to encourage innovation and the
production of nutritionally improved
meat and poultry products.
Some commenters stated that
minimum meat and poultry content
requirements for substitute products are
not necessary so long as the labeling of
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the substitute standardized products
provides sufficient information to
distinguish these products from the
traditional standardized products for
which they substitute. One commenter
submitted data showing that consumers
do not mind if part of the meat block in
a substitute product is replaced with
another ingredient, so long as the
labeling of the substitute standardized
product discloses the presence of the
replacing ingredient. Another
commenter stated that trends in
consumer behavior, which include
reducing the amount of meat consumed
in order to reduce fat intake, strongly
support the argument that consumers
will not be misled by nutrient-modified
food products that contain less meat and
poultry than is required by the
traditional standardized form of the
food. One commenter suggested that a
substitute standardized product with
reductions in its meat or poultry content
should state on its label that, ‘‘in order
to reduce fat, this product contains less
meat than the traditional standardized
product.’’ Some commenters stated that
nutritional equivalency, rather than
meat-content equivalency, should serve
as the basis for defining requirements
for the use of nutrient content claims.
These commenters felt that FSIS should
allow for necessary reductions in meat
or poultry content to meet the
requirements of the claim, with the
reduction accomplished in such a
manner that nutritional equivalency to
the traditional standardized product is
maintained. One commenter stated that
meat replacers may be more desirable
than some of the fat replacers, which
hold water but contribute little in taste
or nutritional value.
One commenter stated that it is
widely recognized that the requirements
for minimum meat content are based on
the notion that meat and poultry
represented the most valuable
constituent of a meat or poultry product.
This commenter claimed that meat and
poultry are simply no longer the
indisputable ‘‘highest value’’
components of food products. Another
commenter mentioned that FDA
regulations provide for marketing of
products, such as reduced-fat peanut
butter, which allows for reduction of the
peanut content of the product below
that required for the standardized
product.
Those commenters that agreed with
the requirement that substitute
standardized products subject to the
general standard maintain the same
minimum meat and poultry requirement
as the standardized product for which
they are a substitute maintained that
consumers have come to expect a
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certain amount of meat or poultry in
products that bear a standardized term,
and that the meat and poultry content
of the product is still the most valued
constituent.
Response: Because many consumers
have come to expect a certain amount of
meat or poultry in products that bear a
standardized term, deviations in the
prescribed meat or poultry content will
not be permitted in this final rule.
Moreover, while FSIS appreciates these
comments, the Agency does not view
this rulemaking as the appropriate
vehicle for changing the specific meat
and poultry content requirements of
meat and poultry product standards.
These issues will be considered in a
separate rulemaking that will examine
FSIS’s overall regulatory approach to
standardized meat and poultry products
that was described in the ANPR ‘‘Meat
and Poultry Standards of Identity and
Composition’’ published in the
September 9, 1996, edition of the
Federal Register (61 FR 47453).
In response to that ANPR, FSIS and
FDA are jointly working on a more
comprehensive approach to
modernizing food standards whose goal
is to establish ‘‘general principles’’ that
interested parties could follow in
requesting changes to food standards.
One change that interested parties may
be able to pursue, if these principles are
adopted, would be reductions in the
meat or poultry content requirements of
standardized products. FSIS and FDA
expect to soon publish the joint
proposed rule in the Federal Register.
Nomenclature-Labeling of Nutrient
Content Claims
Comment: Of those who commented,
all agreed that the name of a substitute
standardized product subject to the
general standard should be an expressed
nutrient content claim in conjunction
with (i.e., next to) the appropriate
standardized term, as provided in the
proposal. However, several commenters
did not agree with the provision in
proposed 9 CFR 319.10(d) and 9 CFR
381.172(d) that states that the nutrient
content claim and standardized term
should be presented ‘‘in the same style,
color, and size of type on the product
label.’’
One commenter stated that it was
unaware of any evidence that
consumers are confused or misled by
the labels currently in the marketplace
on similar FDA-regulated products,
which are not subject to a style, color,
and size of type requirement. The
commenter stated that the 3:1 type size
requirement that generally applies to
names on FSIS-regulated products
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should apply to foods that are marketed
under the general standard rule.
Another commenter stated that some
flexibility should be allowed for the
type size of the nutrient content claim.
The commenter stated that some
product names are fairly lengthy, and
therefore, FSIS’s Policy Memo 87A ,
Word Size in Labeling of Product Names
and Fanciful Names, states that the
Agency will not object to a 1⁄3 type size
flexibility between the largest letter and
the smallest letter in a product name.
The commenter also noted that the
existing FSIS regulations for nutrient
content claims allow a 1⁄2 type size
flexibility to assure that nutrient claims
are not disproportionately larger than
the product’s statement of identity.
Two commenters stated that the FDA
regulation establishing a general
standard for FDA-regulated substitute
standardized products (21 CFR
130.10(e)) does not contain the same
restrictions on the style, color, and size
of type of the nutrient content claim that
FSIS’s proposed rule does. One of these
commenters requested that FSIS
consider modifying the proposed
nomenclature for products subject to its
general standard to make it similar in
format to that prescribed by the FDA
regulation. A similar comment
suggested that FSIS delete the last
clause from the nomenclature section,
i.e., ‘‘ * * * which shall be in the same
style, color, and size of type,’’ because
it is unwarranted and unnecessary to
inform consumers of the nature of the
substitute product.
Response: FSIS agrees with the
commenters’ arguments and in this final
rule has deleted the last clause from the
nomenclature section (‘‘ * * * which
shall be in the same style, color, and
size of type’’). FSIS has been persuaded
by the arguments against requiring the
nutrient content claim portion of the
substitute standardized product’s name
to be presented in the same style, color,
and size of type, as the standardized
product term and agrees that this
requirement is unnecessary for
consumers to distinguish the substitute
product from other products that bear
nutrient content claims but that are not
substitute products that meet the
requirements of this final rule.
Therefore, to harmonize, to the extent
possible, its labeling requirements with
the labeling requirements of FDA’s
corresponding regulations found in 21
CFR 130.10, FSIS will not require that
the expressed nutrient content claim
that is part of the product identity
appear in ‘‘the same style, color, and
size of type’’ as the standardized term.
The product name on the principal
display panel of the substitute product,
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as well as its ingredients statement, are
the pertinent labeling features that
identify the differences between the
traditional standardized product and the
modified version bearing the
standardized name.
Ingredient Labeling
Comment: Twenty commenters
expressed agreement with the provision
in proposed 9 CFR 319.10(e) and
381.172(e) that all safe and suitable
ingredients not provided for by the
traditional standard, as well as
permitted ingredients added at a level in
excess of those allowed by the
traditional standard, must be
appropriately identified as such with an
asterisk in the ingredients statement.
Three commenters disagreed.
Two commenters stated that because
a nutrient content claim calls the
consumer’s attention to the fact that the
product has been modified from the
traditional standardized product, there
is no need for asterisks to be included
in the labeling information. These
commenters believed that the product
name with the appropriate nutrient
content claim, along with the
ingredients statement, is all that is
necessary to adequately inform the
consumer that the product has been
modified from the traditional standard.
One commenter stated that, in addition
to adding to label clutter, the
requirement to highlight ingredients
present in amounts greater than in the
standardized product could result in the
‘‘ludicrous’’ situation where a label
indicates that the substitute product
contains more meat than the traditional
standardized product. The commenter
felt that requiring an asterisks for
particular ingredients will provide a
disincentive for meat and poultry
processors to make products using the
new technologies in fat replacement
products because they must market
products with labels that are cluttered
with additional statements.
One commenter expressed support for
using an asterisk to identify ingredients
not provided for, or used in excess of
those levels provided for, by the
traditional standard in so far as it
provides parity with FDA’s regulation
but questioned the real value of this
labeling feature to the consumer. The
commenter suggested that this labeling
requirement be applicable on a shortterm basis, with provisions for its phaseout in no more than three years as
consumer become more familiarly with
nutritionally-modified foods.
Two commenters felt that FSIS should
require more than just the identification
of the substitute ingredients in the
ingredients listing, as proposed by the
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Agency. These commenters suggested
that FSIS also require that whenever
ingredients are present in the substitute
product that are not permitted by the
traditional product standard, an
appropriate disclosure (e.g. ‘‘made with
non-standard ingredients—see back
panel for ingredient lists’’) appear on
the principal display panel. One of
these commenters stated that such a
disclosure would alert consumers to the
fact that a substitute product is different
from the standardized product and
would direct them to specific
information about the differences.
Several commenters requested that
FSIS clarify whether the ingredient
‘‘water’’ or the added moisture not
normally in or in excess of that
permitted in a standardized product
should be indicated with an asterisk.
Response: FSIS disagrees with the
comment that ingredients not provided
for by the traditional standard, as well
as permitted ingredients added at a level
in excess of those allowed by the
traditional standard, need not be
identified as such with an asterisk in the
ingredients statement. Differences
between the ingredients in a
standardized product and a substitute
standardized product identified in part
by a nutrient content claim must be
highlighted so that consumers will be
able to differentiate between the
traditional standardized product and the
substitute version. Highlighting these
ingredient differences also ensures that
the labeling of the substitute product
will not be misleading. Furthermore, as
a point of clarification, when water or
added moisture not found in or used in
excess of that permitted in a traditional
standardized product is added to a
substitute standardized product, this
fact must be highlighted with an asterisk
as is required for all other safe and
suitable ingredients not found in, or
used in excess of, the amount permitted
by the traditional standard.
FSIS disagrees with the comment that
requiring an asterisks to highlight
specific ingredients present in a
substitute standardized product will
provide a disincentive for meat and
poultry processors to make and
manufacture standardized products
with reductions in their fat content.
Similar labeling has been required on
FDA-regulated products for several
years and does not appear to have been
a disincentive for industry to develop
these kinds of products. FSIS also
disagrees that labeling features in
addition to those provided in the
proposed rule are necessary to inform
consumers of ingredient differences
between a traditional standardized
product and its nutritionally modified
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33813
substitute. Highlighting ingredient
differences with an asterisk in the
ingredients statement, along with the
product name on the principal display
panel, are the pertinent labeling features
that identify the differences between the
traditional standardized product and the
substitute version. Furthermore, to some
consumers, statements such as ‘‘made
with non-standard ingredients’’ may
imply that the ingredients used in a
substitute product are inferior or
harmful to the ingredients used in the
traditional standardized product. Such
statements could be misleading because
only ingredients that have been found to
be safe and suitable for use in meat and
poultry products are permitted to be
used in formulating substitute
standardized products.
Consumers who have purchased
substitute standardized products
manufactured pursuant to FDA’s general
standard codified at 21 CFR 130.10 are
familiar with the labeling of such
products through the use of asterisks
and the statement referenced by the
asterisks, which appear adjacent to the
ingredient list. Thus, many consumers
already look to the ingredient statement
to determine differences in formulation
between traditional standardized
products and nutritionally modified
versions of these products. Harmonizing
labeling to the extent possible with that
of the FDA benefits consumers by
providing a more consistent food
labeling system across all foods.
FSIS finds no merit in the comment
that asterisks are unnecessary because
they could lead to the ‘‘ludicrous’’
situation where an ingredients
statement asterisk would indicate that
more meat or poultry than required by
the food standard has been used in the
product. Because food standards for
meat and poultry products generally
require minimum amounts of meat and
poultry and maximum amounts of fat
and water, it has always been possible
for manufacturers to include more meat
or poultry than the minimum
established by the food standard in the
product formulation. This rule does not
change that fact and there is no need to
require an asterisk to highlight the fact
that a manufacture chose to include
more meat or poultry in a substitute
product than the minimum required by
the traditional standard.
Regarding the comment that the
asterisk provision should be phased out
at some point in the future, FSIS does
not agree with this view because the
ingredient statement is the primary
feature where the differences between
the standardized product and the
substitute version can be made known
to the consumer in labeling. As
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described earlier, during the joint FSIS
and FDA standards modernization
activities, if appropriate, the agencies
may revisit the issue of phasing out the
asterisk requirement and consider it
within the context of a more
comprehensive approach to food
standards modernization.
The Final Rule
In this final rule, FSIS is establishing
a general definition and standard of
identity for standardized meat and
poultry products that have been
modified to qualify for use of an
expressed nutrient content claim in
their product names in conjunction with
a standardized term. FSIS is adding new
§§ 319.10 and 381.172 to the meat and
poultry products regulations in title 9 of
the CFR. As was proposed, §§ 319.10(a)
and 381.172(a) describe the type of meat
and poultry products that are defined by
the general standard. These are products
that substitute, in accordance with 9
CFR 317.313(d) or 381.413(d), for a
standardized product, but that do not
comply with the established standard
because of a compositional deviation
that results from reductions of a
constituent that is described by an
express nutrient content claim, such as
‘‘low fat’’ or ‘‘fat free.’’
As was proposed, §§ 319.10(b) and
381.172(b) require that a substitute
standardized product subject to the
general standard have similar
performance characteristics to the
traditional standardized product for
which it is a substitute. However, if a
substitute product has performance
characteristics that materially limit the
uses of the product compared to the
uses of the traditional standardized
product, §§ 319.10(b) and 381.172(b)
require that a product’s label include a
disclaimer informing consumers of such
differences, such as ‘‘not suitable for
grilling.’’ In response to some of the
comments and to be consistent with the
existing definition of substitute
products found in 9 CFR 317.313 and
381.413, FSIS is removing the provision
in proposed §§ 319.10(b) and 381.172(b)
that would have required the
performance characteristics disclaimer
to appear ‘‘adjacent to the product
name.’’ Deleting this provision is also
intended to provide consistency with 21
CFR 130.10 of the FDA regulations,
which is the codified general standard
of identity for substitute standardized
products under FDA jurisdiction. As
was proposed, §§ 319.10(b) and
381.172(b) will require that deviations
in the ingredients in a substitute
standardized product be the minimum
necessary to qualify for the nutrient
content claim.
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Sections 319.10(c) and 381.172(c)
prescribe the ingredients that must be
used in, and the ingredients that are
permitted to be used in, substitute
standardized products under the general
standard. As was proposed,
§§ 319.10(c)(1) and 381.172(c)(1) require
that the ingredients used in a substitute
standardized product be those
ingredients provided for by the
traditional standard, except that in
addition, safe and suitable ingredients
may be used in the substitute product at
the minimum level necessary to
improve texture or prevent synereses.
The final rule replaces references to
former §§ 318.7 and 381.147 with the
phrase ‘‘as provided in a regulation
permitting that use in this subchapter or
in 9 CFR Chapter III, Subchapter E, or
in 21 CFR Chapter I, Subchapter A or
Subchapter B,’’ to reflect the issuance of
the final rule ‘‘Food Ingredients and
Sources of Radiation Listed or
Approved for Use in Meat and Poultry
Products’’ (64 FR 72168).
As was proposed, §§ 319.10(c)(2) and
381.172(c)(2) forbid substitute
standardized products to replace or
exchange ingredients required by the
traditional standard with functionally
similar ingredients from other sources
not provided for in the traditional
standard. In the final rule, FSIS is
removing the phrases ‘‘textured
vegetable protein shall not replace
meat’’ and ‘‘textured vegetable protein
shall not replace poultry’’ from
proposed §§ 319.10 (c)(2) and
381.172(c)(2). These phrases are
unnecessary and could potentially cause
confusion since the final rule permits
TVP to be used in limited amounts as
a fat replacer, although it may not be
used to replace meat. Reductions in the
meat or poultry content required by the
traditional standard are already
prohibited by the final rule regardless of
whether TVP is used in the product.
As was proposed, §§ 319.10(c)(3) and
381.172(c)(3) prohibit substitute
standardized products from containing
ingredients that are prohibited for use in
traditional standardized products.
Proposed §§ 319.10(c)(2) and(3), and
381.172(c)(2) and (3) use the phrase
‘‘[a]n ingredient or component of an
ingredient’’ when describing the
ingredients permitted and prohibited in
substitute standardized products. In this
final rule, FSIS is deleting the words ‘‘or
component of an ingredient’’ because
they are unnecessary and may cause
confusion.
Proposed, §§ 319.10(c)(4) and
381.172(c)(4) required substitute
standardized products to conform to
certain aspects of the traditional
standard, such as the meat or poultry
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content specified in the standard, the
anatomic location and kind of meat or
poultry specified in the standard, and
the processing procedures specified in
the standard. As previously mentioned,
deviations from these types of
requirements may result in a product
that is so physically dissimilar from the
traditional standardized product that it
does not come within the established
definition of a substitute product.
However, because certain
technologies used to prepare
standardized foods may yield a product
with the same physical, nutritional, and
sensory characteristics as the food made
in accordance with the traditional
standards, FSIS intends to consider
certain deviations from product
standards, such as alternative
processing methods, on a case-by-case
basis. As stated above, FSIS and FDA
are jointly working on a more
comprehensive approach to
modernizing food standards to establish
‘‘general principles’’ that interested
parties would follow in requesting
changes to or creating new food
standards. Therefore, FSIS is revising
proposed §§ 319.10(c)(4) and
381.172(c)(4) to require that substitute
standardized products comply with all
other applicable standards of identity or
composition unless otherwise specified
in part 319 or part 381. The Agency is
making this revision to accommodate
changes to food standards that may
result from the joint FSIS/FDA food
standards modernization approach.
As was proposed, §§ 319.10(c)(5) and
381.172(c)(5) permit water and fatreplacing binders to be used to reduce
the fat content in a substitute
standardized product subject to the
general standard. Based on the
comments and data submitted in
response to the proposal in support of
using TVP as a ‘‘fat replacer,’’ FSIS will
permit the use of TVP as a functional fat
replacing ingredient in substitute
standardized products defined by the
general standard. FSIS is adding new
language to the final rule that permits
the use of TVP as part of a fat
replacement system at the lowest level
necessary to achieve the technical effect
of replacing the characteristics of fat in
the substitute product. This language is
found in new §§ 319.10(c)(6) and
381.172(c)(6). Because §§ 319.10(c)(2)
and 381.172(c)(2) of the final rule forbid
reductions in the meat or poultry
content of a substitute product where
one is established by a standard, under
the final rule, TVP may only be used to
replace fat component and not to
replace the lean meat or poultry content
of the substitute standardized product.
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Sections 319.10(d) and 381.172(d)
prescribe the nomenclature for the
substitute meat and poultry products
that comply with the general standard.
As was proposed, these products may be
identified by the appropriate expressed
nutrient content claim and the
applicable standardized term (e.g., ‘‘Fat
Free Bologna’’). If a product meets the
requirements of the general standard, it
is itself a standardized product, and
therefore, its name will not be required
to contain the term ‘‘substitute’’ despite
the fact that it does not meet all of the
requirements of the traditional product
standard.
This final rule removes the provisions
in proposed §§ 319.10(d) and 381.172(d)
that would have required that the
expressed nutrient content claim part of
the substitute standardized product’s
name appear in the ‘‘same style, color
and size type’’ as the standardized term.
This change is in response to public
comments and to harmonize, to the
extent possible, with similar FDA
regulations.
As was proposed, §§ 319.10(e) and
381.172(e) require each of the
ingredients used in the substitute
product to be declared on the product
label as required by the applicable FSIS
regulations. 9 CFR parts 317 and 381,
subpart N, require that all ingredients be
listed by common or usual name in
descending order of predominance by
weight. As was proposed, §§ 319.10(e)
and 381.172(e) also require that all safe
and suitable ingredients not provided
for by the traditional standard, as well
as those used in excess of those
permitted by the traditional standard, be
identified as such with and asterisks in
the ingredients statement.
Executive Order 12866 and Regulatory
Flexibility Act
This rule has been determined to be
significant and therefore has been
reviewed by OMB under EO 12866.
I. Need for the Rule
FSIS is issuing this rule to facilitate
the development and availability of
substitute standardized products that
have reductions in certain constituents
that are of health concern to some
consumers, such as fat, cholesterol, and
sodium. This rule allows FSIS to rely
more on labeling requirements and less
on restrictive recipe-like standards in
endeavoring to ensure that the labels of
meat and poultry products are truthful
and not misleading as well as to
improve the public health. The names of
products covered by the General
Standard will be composed of an
express nutrient content claim that
reflects the modifications made in
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formulating and processing the product
(so that it qualifies to bear the claim)
and an established standardized term.
FDA has already promulgated a
corresponding General Standard for the
products that it regulates (21 CFR
130.10). By harmonizing an FSIS
labeling requirement with that of FDA,
this final rule represents a significant
step towards providing consumers with
an informative and consistent food
standard and labeling system. This final
rule also promotes product innovation
by encouraging the production of meat
and poultry products that are low in
constituents that are of health concern
to some people.
II. Description of Affected Industry
FSIS regulations contain
approximately 80 standards of identity
or composition for meat and poultry
products. Most of these standards are for
processed products, including sliced,
injected, smoked, fermented, heattreated, and raw products. According to
the Agency’s Performance Based
Inspection System Database, in the
second quarter of 2003, there were
approximately 6,600 Federal and State
Establishments 2 that potentially will be
affected by the final rule if they develop
and make available substitute products
for standardized products. Some of
these establishments, however, are
already producing sausage and other
comminuted meat and poultry products
under FSIS Policy Memo 121B and
Policy Memo 123 which provide for the
type of substitute products defined
under this final rule. Thus, this rule is
likely to have little or no impact on the
processing establishments that are
producing products in accordance with
the policy memos.
Ingredient manufacturers who
produce binders and textured (source)
protein products (e.g., textured soy or
wheat protein) will be affected by the
final rule because the rule will permit
the increased use of these ingredients as
fat replacing ingredients in some
modified standardized products.
III. Costs
The decision to produce products
subject to the General Standard
established by this rule is voluntary.
Therefore, only those manufacturers
that choose to produce and market these
products will incur the direct costs
imposed by this rule. These costs
include research and development,
production and marketing, and labeling
production. However, because the rule
is voluntary, companies that choose to
2 These establishments processed, froze, stored, or
otherwise held meat and poultry products.
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33815
produce products covered by the
General Standard will do so only if they
determine that the benefits of producing
and selling these products outweigh the
costs of complying with the final rule.
Furthermore, companies that are already
producing and marketing products
under Policy Memo 121B and Policy
Memo 123 (i.e., comminuted meat and
poultry products) are likely to incur
minimal or no costs as a result of this
final rule.
Under most circumstances,
companies are likely to charge a
premium for substitute standardized
product produced in compliance with
this final rule because many consumers
will be willing to pay a premium for
products with improved nutritional
profiles. They view these products as
‘‘value added’’ products.3 Therefore,
based on the experience of food
companies that are operating under
FDA’s 21 CFR 130.10 regulations, e.g.,
the manufacturers of fat-free ice cream
and reduced fat cream cheese, any costs
associated with producing and
marketing substitute products most
likely will be passed on to the consumer
in the form of higher retail prices.
However, once this rule becomes
effective, some companies that are not
producing substitute meat and poultry
products under Policy Memo 121B or
Policy Memo 123 may begin to
manufacture and market substitute
standardized products in accordance
with the General Standard because of
the market value of using traditional
product names. Their decision to do so
could have the effect of increasing the
supply of these types of products in the
short run, which could translate into
lower prices for consumers.
IV. Benefits
This rule will assist consumers in
making dietary choices by providing for
modified versions of standardized meat
and poultry products that have
reductions of certain constituents that
are of health concern to some
consumers, such as fat, cholesterol, and
sodium. Therefore, there will be a
greater opportunity for consumers to
maintain or to initiate healthy dietary
practices. In the United States, diets
high in fat, cholesterol, and sodium are
associated with chronic diseases such as
coronary heart disease, cancer, stroke,
and diabetes. In 2002, according to the
Centers for Disease Control National
Center for Chronic Disease Prevention
and Health Promotion, 7 out of every 10
U.S. deaths and more than 60% of
medical care expenditures are attributed
to chronic diseases. In addition, the
3 Consumer
E:\FR\FM\10JNR1.SGM
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33816
Federal Register / Vol. 70, No. 111 / Friday, June 10, 2005 / Rules and Regulations
prolonged illness and disability
associated with many chronic diseases
decrease the quality of life for millions
of consumers.
ESTIMATED DIRECT AND INDIRECT COSTS OF CARDIOVASCULAR DISEASES, STROKE, DIABETES, AND CANCER IN THE
UNITED STATES—2002
[In Billion of Dollars]
Cardiovascular
diseases
Costs
Stroke
Diabetes
Cancer
Direct ................................................................................................................
Indirect .............................................................................................................
$168.7
111.1
$30.8
18.6
$92.0
40.0
$61.0
111.0
Total ..........................................................................................................
279.8
49.4
132.0
172.0
billion, respectively, as reflected in the
above table and figure 1 below. Direct
costs ($168.7 billion and $30.8 billion,
respectively) consist of the cost of
physicians and other health
professionals, hospital and nursing
home services, medication, home health
care, and other medical durables.
Indirect costs ($111.1 billion and 18.6
billion, respectively) consist of lost
productivity resulting from morbidity
and mortality.
The total cost in 2002 associated with
diabetes was $132 billion of which $92
billion were direct costs and $40 billion
were indirect costs.4 The estimated total
costs for all cancers in 2002 were $172
billion ($61 billion in direct costs and
$110 billion in indirect costs) 5.
Most chronic diseases are
preventable, or their onset can be
delayed, through increased physical
activity and healthy eating. There is
research to support that practicing good
nutrition lowers the risk of chronic
diseases for many consumers.6 The total
estimated cost of chronic diseases to the
consumer is $633.2 billion. The extent
to which these costs might be reduced
by an improved diet cannot be
calculated precisely, but some
researchers estimate that a balanced and
healthful diet might forestall at least 20
percent of the annual deaths from heart
disease, stroke, cancer, and diabetes.7
It is reasonably expected that the final
rule could contribute to the reduction of
these costs, but this contribution, too,
cannot be calculated precisely. In the
‘‘Economic Benefits of Nutrition
Labeling: A Case Study for Fresh Meat
and Poultry Products,’’ the Agency
estimated the potential benefits of
reducing the incidence of coronary heart
disease and three types of cancers at
$61.8 million, (7 percent discount rate);
and $125 million (3 percent discount
rate).8
The results of the 2002 ‘‘Trends’’
survey’’ conducted by the Food
4 ‘‘The
Economic Costs of Diabetes in the U .S.
2002’’, American Diabetes Association.
5 Heart Disease and Stroke Statistics—2003
Update, American Heart Association.
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6 CDC National Center for Chronic Disease
Prevention and Health Promotion, ‘‘Physical
Activity and Good Nutrition: Essential Elements to
Prevent Chronic Diseases and Obesity.’’
7 ‘‘The American Diet: A Costly Health Problem,
Food Review.’’
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8 The Agency estimated the potential benefit of an
FSIS rule (2001). Nutrition Labeling of ground or
chopped meat and poultry products and singleingredient products. Federal Register, 66, 4969–
4999.
E:\FR\FM\10JNR1.SGM
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ER10JN05.003
According to the 2002 Heart and
Stroke Statistical Update published by
the American Heart Association and the
American Stroke Association, the total
cost of cardiovascular diseases and
strokes in the United States was
estimated at $279.8 billion and $49.4
Federal Register / Vol. 70, No. 111 / Friday, June 10, 2005 / Rules and Regulations
Marketing Institute (Trends in the
United States, Consumer Attitudes and
the Supermarket) stated that 80 percent
of consumers surveyed indicated that
they had sought out and purchased
products based on ‘‘low-fat’’ claims; 60
percent had purchased products
because of ‘‘low cholesterol’’ claims; 59
percent purchased products because of
‘‘natural’’ claims; and 52 percent
purchased products because of ‘‘low
salt’’ claims. If this trend continues, and
the final rule is promulgated, it is more
than likely that the final rule will assist
in the reduced incidence of chronic
diseases by expanding the availability of
meat and poultry products with lower
levels of constituents such as fat,
cholesterol, and sodium.
In conclusion, this final rule will
assist consumers who want to reduce
their dietary intake of fat, cholesterol,
and sodium by encouraging the
production of modified versions of
traditional meat and poultry products
that are formulated with fat, cholesterol,
and sodium-replacing ingredient
systems that reduce these constituents.
The final rule will provide parity with
FDA’s regulations and will promote a
unified approach to food standards and
labeling. Most importantly, the final
rule supports national efforts to reduce
the expenditures for health care and the
cost of morbidity and lost productivity
by permitting the introduction of
modified, substitute foods.
In terms of administrative benefits,
the General Standard established by this
final rule will permit industry to
introduce modified, substitute versions
of traditional standardized meat and
poultry products without having to
petition FSIS to establish new standards
for products on a case-by-case basis.
This will generate efficiency within the
food standards system by saving time
and resources that would have been
expended by both the industry and FSIS
to establish new or modified product
standards. It will also permit companies
to introduce standardized meat and
poultry products with improved
nutritional profiles into the marketplace
in a timely manner, making such
products more readily available to
consumers.
V. Regulatory Flexibility Analysis
The FSIS Administrator has made a
final determination that this rule will
not have a significant economic impact
on a substantial number of small
entities, as defined by the Regulatory
Flexibility Act (5 U.S.C. 601).
This final rule will not impose any
new requirements on small entities. The
decision to produce versions of
standardized products that have been
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modified to qualify for use of an
expressed nutrient content claim in
conjunction with a traditional product
name is voluntary. Therefore, the
requirements of this final rule will only
apply to those small manufacturers who
choose to produce these types of
products. Those small entities that
choose to produce these products will
be required to design new labels or to
revise current labels to comply with this
new rule, and thereby incur some costs.
However, small entities who will be
marketing these substitute products will
most likely have anticipated that the
revenues generated from the sale of
these products will outweigh the costs
of complying with the new regulation.
Executive Order 12988
This final rule has been reviewed
under Executive Order 12988, Civil
Justice Reform. This final rule: (1)
Preempts State and local laws and
regulations that are inconsistent with
this rule; (2) has no retroactive effect;
and (3) does not require administrative
proceedings before parties may file suit
in court challenging this rule. However,
the administrative procedures specified
in 9 CFR 306.5, 381.35, and 590.320
through 590.370 must be exhausted
before any judicial challenge of the
application of the provisions of this
rule, if the challenge involves any
decision of an FSIS employee relating to
inspection services provided under the
FMIA or PPIA.
Paperwork Reduction Act
In accordance with section 3507(j) of
the Paperwork Reduction Act of 1995
(44 U.S.C. 3501 et seq.), FSIS will
submit the information collection and
recordkeeping requirements in this final
rule to the Office of Management and
Budget (OMB) for approval.
Title: Food Standards: Requirements
for Substitute Standardized Meat and
Poultry Products Named by Use of an
Expressed Nutrient Content Claim and a
Standardized Term.
Type of collection: New.
Abstract: Under this final rule, FSIS is
requiring that establishments that
produce meat and poultry products in
accordance with the definition and
general standard of identity for
substitute standardized products design
new product labels and submit sketches
of the new labeling to FSIS for approval.
To receive approval of the labels,
establishments must complete FSIS
form 7234–1. FSIS employees review
FSIS form 7234–1 to ensure that
information on the labels complies with
the regulations.
Estimate of burden: FSIS estimates
that it will take 60 minutes to design
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33817
and develop modified product labels in
accordance with the final regulations
and 15 minutes to prepare FSIS form
7234–1 and submit it, along with the
label, to FSIS.
Respondents: Establishments that
produce substitute standardized meat or
poultry products in accordance with
this final rule.
Estimated Number of Respondents:
100.
Estimated Number of Responses per
Respondent: 5.
Estimated Total Annual Burden on
Respondents: 625 hours.
Copies of this information collection
assessment can be obtained from John
O’Connell, Paperwork Reduction Act
Coordinator, Food Safety and Inspection
Service, USDA, 112 Annex, 300 12th
Street, SW., Washington, DC 20250.
Comments are invited on (a) Whether
the collection of information is
necessary for the proper performance of
the functions of the Agency, including
whether the information will have
practical utility; (b) the accuracy of the
Agency’s estimate of the burden of the
collection of information, including the
validity of the methodology and
assumptions used; (c) ways to enhance
the quality, utility, and clarity of the
information to be collected, ways to
minimize the burden of the collection of
information on those who are to
respond, including through the use of
appropriate automated, electronic,
mechanical, or other technological
collection techniques, or other forms of
information technology. Comments may
be sent to both John O’Connell,
Paperwork Reduction Act Coordinator,
at the address provided above, and the
Desk Officer for Agriculture, Office of
Information and Regulatory Affairs,
Office of Management and Budget,
Washington, DC 20253. To be most
effective, comments should be sent to
OMB within 30 days of publication.
Additional Public Notification
Public awareness of all segments of
rulemaking and policy development is
important. Consequently, in an effort to
ensure that the public and in particular
minorities, women, and persons with
disabilities, are aware of this final rule,
FSIS will announce it on-line through
the FSIS Web page located at https://
www.fsis.usda.gov/
regulations_&_policies/
2005_Interim_&_Final_Rules_Index/
index.asp. The Regulations.gov Web site
is the central online rulemaking portal
of the United States government. It is
being offered as a public service to
increase participation in the Federal
government’s regulatory activities. FSIS
participates in Regulations.gov and will
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Federal Register / Vol. 70, No. 111 / Friday, June 10, 2005 / Rules and Regulations
improve texture and prevent syneresis,
2. Part 319, subpart A is amended by
adding a new § 319.10 to read as follows: so that the substitute product is not
inferior in performance characteristics
§ 319.10 Requirements for substitute
from the standardized product defined
standardized meat food products named by
in this part for which it is a substitute.
use of an expressed nutrient content claim
(2) An ingredient that is specifically
and a standardized term.
required by the standard prescribed in
(a) Description. The meat food
this part shall not be replaced or
products prescribed by this general
exchanged with a similar ingredient
definition and standard of identity are
from another source, for example, turnip
those products that substitute, in
chunks shall not replace potatoes in
accordance with § 317.313(d), for a
corned beef hash.
standardized product defined in this
(3) An ingredient that is specifically
part and use the name of that
prohibited from use in any meat food
standardized product in their statements product by this part shall not be added
of identity, but that do not comply with to the substitute meat food product
the established standard because of a
under this section.
compositional deviation that results
(4) Unless otherwise specified in this
from reduction of a constituent that is
part, a substitute meat food product
described by an expressed nutrient
must meet all other requirements of the
content claim that has been defined by
applicable standards of identity or
regulation in part 317, subpart B, of this composition.
subchapter. The expressed nutrient
(5) Water and fat-replacers (e.g.,
content claim shall comply with the
binders), in combination, may be added
requirements of § 317.313 of this
to replace fat in accordance with
subchapter and with the requirements of paragraph (c) of this section.
part 317, subpart B, of this subchapter
(6) Textured vegetable protein may be
which define the particular nutrient
used by itself or in combination with
content claim that is used. The meat
other binders and water as a fat replacer
in accordance with paragraph (c) of this
food product shall comply with the
relevant standard in this part in all other section.
(d) Nomenclature. The name of a
respects, except as provided in
substitute meat food product that
paragraphs (b) and (c) of this section.
complies with all parts of this section is
(b) Performance characteristics. The
the appropriate expressed nutrient
performance characteristics, such as
content claim and the applicable
physical properties, functional
standardized term.
properties, and shelf-life, of the meat
(e) Label declaration. (1) Each of the
food product shall be similar to those of
ingredients used in the substitute meat
the standardized meat food product
food product shall be declared on the
produced under this part. If there is a
label as required by this section and part
significant difference in a performance
317 of this subchapter.
characteristic that materially limits the
(2) Ingredients not provided for, and
use of the product compared to the use
ingredients used in excess of those
of the standardized product defined in
levels provided for, by the standard as
this part, the label shall include a
defined in this part, shall be identified
statement in accordance with
as such with an asterisk in the
§ 317.313(d)(1) and (2) of this
subchapter that informs the consumer of ingredients statement. The statement
List of Subjects
‘‘*Ingredients not in regular llll’’
such differences (e.g., if appropriate,
(the blank shall be filled in with the
‘‘not recommended for frozen storage’’
9 CFR Part 319
name of the traditional standardized
or ‘‘not suitable for roller grilling’’).
Food grades and standards, Meat
product) or ‘‘**Ingredients in excess of
Deviations from the ingredient
inspection.
amounts permitted in regular llll’’
provisions of the standard must be the
(the blank shall be filled in with the
9 CFR Part 381
minimum necessary to qualify for the
name of the traditional standardized
nutrient content claim, while
Food grades and standards, Meat
product), or both, as appropriate, shall
maintaining similar performance
inspection, Poultry and poultry
immediately follow the ingredients
characteristics.
products.
statement in the same type and size.
(c) Ingredients used in substitute
I For the reasons stated in the preamble,
products. (1) Ingredients used in the
FSIS amends 9 CFR parts 319 and 381 as product shall be those ingredients
PART 381—POULTRY PRODUCTS
follows:
INSPECTION REGULATIONS
provided for in the standard as defined
in this part, except that safe and suitable I 3. The authority citation for part 381
PART 319—DEFINITIONS AND
ingredients permitted for use in meat
would continue to read as follows:
STANDARDS OF IDENTITY OR
food products as provided in a
COMPOSITION
Authority: 7 U.S.C. 138f; 450, 21 U.S.C.
regulation permitting that use in this
451–470, 7 CFR 2.18, 2.53.
I 1. The authority citation for part 319
subchapter or in 9 CFR Chapter III,
continues to read as follows:
Subchapter E, or in 21 CFR Chapter I,
I 4. Part 381, subpart P is amended by
Subchapter A or Subchapter B, may be
adding a new § 381.172 to read as
Authority: 7 U.S.C. 450, 1901–1906; 21
used at the minimum level necessary to follows:
U.S.C. 601–695; 7 CFR 2.18, 2.53.
accept comments on documents
published on the site. The site allows
visitors to search by keyword or
Department or Agency for rulemakings
that allow for public comment. Each
entry provides a quick link to a
comment form so that visitors can type
in their comments and submit them to
FSIS. The Web site is located at
https://www.regulations.gov/.
FSIS also will make copies of this
Federal Register publication available
through the FSIS Constituent Update,
which is used to provide information
regarding FSIS policies, procedures,
regulations, Federal Register notices,
FSIS public meetings, recalls, and other
types of information that could affect or
would be of interest to our constituents
and stakeholders. The update is
communicated via Listserv, a free e-mail
subscription service consisting of
industry, trade, and farm groups,
consumer interest groups, allied health
professionals, scientific professionals,
and other individuals who have
requested to be included. The update
also is available on the FSIS Web page.
Through Listserv and the Web page,
FSIS is able to provide information to a
much broader, more diverse audience.
In addition, FSIS offers an email
subscription service which provides an
automatic and customized notification
when popular pages are updated,
including Federal Register publications
and related documents. This service is
available at https://www.fsis.usda.gov/
news_and_events/email_subscription/
and allows FSIS customers to sign up
for subscription options across eight
categories. Options range from recalls to
export information to regulations,
directives and notices. Customers can
add or delete subscriptions themselves
and have the option to password protect
their account.
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Federal Register / Vol. 70, No. 111 / Friday, June 10, 2005 / Rules and Regulations
§ 381.172 Requirements for substitute
standardized poultry products named by
use of an expressed nutrient content claim
and a standardized term.
(a) Description. The poultry products
prescribed by this general definition and
standard of identity are those products
that substitute, in accordance with
§ 381.413(d), for a standardized product
defined in this subpart and use the
name of that standardized product in
their statements of identity, but that do
not comply with the established
standard because of a compositional
deviation that results from reduction of
a constituent that is described by an
expressed nutrient content claim that
has been defined by regulation in this
subpart. The expressed nutrient content
claim shall comply with the
requirements of § 381.413 and with the
requirements in subpart Y of this part
which define the particular nutrient
content claim that is used. The poultry
product shall comply with the relevant
standard in this part in all other
respects, except as provided in
paragraphs (b) and (c) of this section.
(b) Performance characteristics. The
performance characteristics, such as
physical properties, functional
properties, and shelf-life, of the poultry
product shall be similar to those of the
standardized poultry product produced
under subpart P of this part. If there is
a significant difference in a performance
characteristic that materially limits the
use of the product compared to the use
of the standardized product defined in
subpart P of this part, the label shall
include a statement in accordance with
§ 381.413(d)(1) and (2) of this part, that
informs the consumer of such
differences (e.g., if appropriate, ‘‘not
recommended for frozen storage’’ or
‘‘not suitable for roller grilling’’).
Deviations from the ingredient
provisions of the standard must be the
minimum necessary to qualify for the
nutrient content claim, while
maintaining similar performance
characteristics.
(c) Ingredients used in substitute
products. (1) Ingredients used in the
product shall be those ingredients
provided for in the standard as defined
in subpart P of this part, except that safe
and suitable ingredients permitted for
use in poultry products as provided in
a regulation permitting that use in this
subchapter or in 9 CFR Chapter III,
Subchapter E, or in 21 CFR Chapter I,
Subchapter A or Subchapter B, may be
used at the minimum level necessary to
improve texture and prevent syneresis,
so that the substitute product is not
inferior in performance characteristics
from the standardized product defined
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Jkt 205001
in subpart P of this part for which it is
a substitute.
(2) An ingredient that is specifically
required by the standard prescribed in
subpart P of this part shall not be
replaced or exchanged with a similar
ingredient from another source, for
example, extruded turnips shall not
replace noodles in poultry with noodles.
(3) An ingredient that is specifically
prohibited from use in any poultry
product by subpart P of this part shall
not be added to the substitute poultry
product under this section.
(4) Unless otherwise specified in this
part, a substitute poultry product must
meet all other requirements of the
applicable standards of identity or
composition.
(5) Water and fat-replacers (e.g.,
binders), in combination, may be added
to replace fat in accordance with
paragraph (c) of this section.
(6) Textured vegetable protein may be
used by itself or in combination with
other binders and water as a fat replacer
in accordance with paragraph (c) of this
section.
(d) Nomenclature. The name of a
substitute poultry product that complies
with this section is the appropriate
expressed nutrient content claim and
the applicable standardized term.
(e) Label declaration. (1) Each of the
ingredients used in the substitute
poultry product shall be declared on the
label as required by this section and
subpart N of this part.
(2) Ingredients not provided for, and
ingredients used in excess of those
levels provided for, by the standard as
defined in subpart P of this part, shall
be identified as such with an asterisk in
the ingredients statement. The statement
‘‘*Ingredients not in regular llll’’
(the blank shall be filled in with the
name of the traditional standardized
product) or ‘‘**Ingredients in excess of
amounts permitted in regular llll’’
(the blank shall be filled in with the
name of the traditional standardized
product), or both, as appropriate, shall
immediately follow the ingredients
statement in the same type and size.
Done in Washington, DC, on June 6, 2005.
Barbara J. Masters,
Acting Administrator.
[FR Doc. 05–11493 Filed 6–9–05; 8:45 am]
BILLING CODE 3410–DM–P
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33819
NUCLEAR REGULATORY
COMMISSION
10 CFR Parts 170 and 171
RIN 3150–AH61
Revision of Fee Schedules; Fee
Recovery for FY 2005
Nuclear Regulatory
Commission.
AGENCY:
ACTION:
Final rule; correction.
SUMMARY: This document corrects a
final rule appearing in the Federal
Register on May 26, 2005 (70 FR 30526)
concerning the licensing, inspection,
and annual fees charged to NRC
applicants and licensees in compliance
with the Omnibus Budget
Reconciliation Act of 1990, as amended.
This action is necessary to correct
typographical and printing errors.
EFFECTIVE DATE:
July 25, 2005.
FOR FURTHER INFORMATION CONTACT:
Tammy Croote, telephone 301–415–
6041; Office of the Chief Financial
Officer, U.S. Nuclear Regulatory
Commission, Washington, DC 20555–
0001.
SUPPLEMENTARY INFORMATION:
1. On page 30531, in the first column,
under Response, in the fourteenth line,
the word ‘‘commenters?’’ is corrected to
read ‘‘commenters.’’
2. On page 30535, in the second
column, under 4. Charging Fees for
Unlicensed Sites in Decommissioning,
in the eleventh line, the word
‘‘licensees?’’ is corrected to read
‘‘licensees.’’
3. On page 30537, in TABLE III.—
REBASELINED ANNUAL FEES FOR FY
2005, the first number under the FY
2005 Annual Fee column ‘‘$3,115,000’’
is corrected to read ‘‘$3,155,000.’’
4. On page 30540, in the second
column, in the fourth line of the
continued paragraph under Table VIII,
the number ‘‘$2,966,000’’ is corrected to
read ‘‘$2,996,000.’’ Also, in the tenth
line in the same paragraph, the number
‘‘$3,115,000’’ is corrected to read
‘‘$3,155,000.’’
PART 170—[AMENDED]
§ 170.31
[Corrected]
5. On page 30547, in § 170.31, in the
table entitled SCHEDULE OF
MATERIALS FEES, the Category of
materials licenses and type of fees
column entry for 14.B. ‘‘(insert date 1
year from effective date of final rule)’’ is
corrected to read ‘‘July 25, 2006.’’
I
E:\FR\FM\10JNR1.SGM
10JNR1
Agencies
[Federal Register Volume 70, Number 111 (Friday, June 10, 2005)]
[Rules and Regulations]
[Pages 33803-33819]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 05-11493]
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DEPARTMENT OF AGRICULTURE
Food Safety and Inspection Service
9 CFR Parts 319 and 381
[Docket No. 92-024F]
Rin 0583-AC82
Food Standards: Requirements for Substitute Standardized Meat and
Poultry Products Named by Use of an Expressed Nutrient Content Claim
and a Standardized Term
AGENCY: Food Safety and Inspection Service, USDA.
ACTION: Final rule.
-----------------------------------------------------------------------
[[Page 33804]]
SUMMARY: The Food Safety and Inspection Service (FSIS) is amending the
Federal meat and poultry products inspection regulations to establish a
general definition and standard of identity for standardized meat and
poultry products that have been modified to qualify for use of an
expressed nutrient content claim in their product names. These products
will be identified by an expressed nutrient content claim, such as
``fat free,'' ``low fat,'' and ``light,'' in conjunction with an
appropriate standardized term, e.g., ``low fat bologna.'' FSIS is
taking this action to: Assist consumers in maintaining healthy dietary
practices by providing for modified versions of standardized meat and
poultry products that have reductions of certain constituents that are
of health concern to some consumers, such as fat, cholesterol, and
sodium; increase regulatory flexibility and support product innovation,
and provide consumers with an informative nutrition labeling system.
DATES: This final rule will be effective January 1, 2008, the uniform
compliance date for all meat and poultry products subject to labeling
regulations issued by FSIS between January 1, 2005 and December 31,
2006. However, establishments may begin to produce meat and poultry
products in compliance with this final rule anytime before the
effective date.
FOR FURTHER INFORMATION CONTACT: Dr. Robert Post, Director, Labeling
and Consumer Protection Staff, Office of Policy, Program, and Employee
Development, Food Safety and Inspection Service, U.S. Department of
Agriculture, Washington, DC 20250-3700; (202) 205-0279.
SUPPLEMENTARY INFORMATION:
Background
On December 29, 1995, FSIS published a proposed rule in the Federal
Register to amend the Federal meat and poultry products inspection
regulations to establish a general definition and standard of identity
(the ``general standard'') for standardized meat and poultry products
that have been modified to qualify for use of an expressed nutrient
content claim in their product names (60 FR 67474). Under the proposed
general standard, meat and poultry products with a regulatory standard
of identity or composition in 9 CFR Parts 319 and 381, subpart P, would
be permitted to be formulated and processed with ingredients otherwise
not provided for, or in amounts greater than, that allowed by the
standard in order to qualify for certain expressed nutrient content
claims permitted in 9 CFR 317 subpart B and 381, subpart Y, such as
``fat free,'' ``low fat,'' and ``light.'' Instead of being identified
as ``substitute'' standardized meat and poultry products, as required
by the current regulations (9 CFR 317.313(d) and 381.413(d)),
standardized meat and poultry products formulated or processed in
accordance with the proposed general standard could be identified by an
expressed nutrient content claim in conjunction with the standardized
term.
To allow modified versions of standardized meat and poultry
products that have been formulated to reduce their fat content to be
marketed without having to be labeled as ``substitutes,'' FSIS issued
Policy Memo 123, ``Modified Breakfast Sausage, Cooked Sausage, and
Fermented Sausage Products Identified by a Nutrient Content Claim and a
Standardized or Traditional Name,'' and Policy Memo 121B ``Labeling of
Low Fat Ground Beef and Low Fat Hamburger Containing Added
Ingredients,'' in January of 1995. These policy memoranda stated, among
other things, that these products are permitted to be identified by a
nutrient content claim that reflects the reduction in fat content in
the product in conjunction with the appropriate standardized product
name, e.g., ``Fat Free Bologna,'' ``Low Fat Pepperoni,'' or ``Low Fat
Hamburger, Water, and Carrageenan Product.'' Both Policy Memo 121B and
Policy Memo 123 were issued as interim measures until such time that
rulemaking could be completed. Both of these policy memoranda will be
rescinded by this final rule.
In this final rule, FSIS is establishing a general definition and
standard of identity for modified versions of meat and poultry products
that substitute for meat and poultry products defined by a regulatory
standard of identity or composition in 9 CFR Part 319 and 381, subpart
P, i.e., ``substitute standardized products.'' This rule is needed to
facilitate the development and availability of substitute standardized
meat and poultry products that have reductions in constituents that are
of health concern to some people, e.g., fat, cholesterol, and sodium.
The rule allows FSIS to rely more on labeling requirements and less on
restrictive recipe-type standards to carry out its mandate to ensure
that the labels of meat and poultry products are truthful and not
misleading to consumers.
Comments and Agency Response
FSIS received 56 comments in response to the proposed rule from
members of the meat and poultry processing industry, industry trade
associations, members of the flavoring and ingredients industry,
members of the soybean industry, academia, health professionals,
governmental entities, consumer advocacy groups, and individual
consultants. In general, the comments submitted in response to the
proposed rule were favorable. Most commenters agreed that FSIS should
establish a regulatory general standard for substitute standardized
products that are lower in fat, cholesterol, or sodium.
One commenter opposed the rule because the commenter believed it
did not go far enough in providing flexibility to industry. This
commenter stated that, rather than converting FSIS Policy Memo 123 into
regulation, FSIS should create a new standard for substitute
standardized meat and poultry products to allow the use of non-
traditional ingredients in all products, not just versions of products
that are identified by a nutrient content claim and a standardized
product name.
Response: FSIS recognizes the need to explore this and other issues
concerning reform of the meat and poultry product standards. However,
expanding the use of non-traditional ingredients for all standardized
products is an issue that is outside the scope of this rulemaking. The
Agency is, however, exploring this and other related issues in a
separate rulemaking to modernize meat and poultry product standards.
This rulemaking is discussed in greater detail later in this document.
Policy Memo 123 and Policy Memo 121B
Comment: A few commenters felt that FSIS Policy Memo 121B and
Policy Memo 123 should remain in effect once this final rule becomes
effective so that products produced under these policies can continue
to be manufactured. Other commenters stated that the general standard
defined in the proposed rule should apply to food products whose
standards are documented in the FSIS Food Standards and Labeling Policy
Book (the Policy Book), as well as those products whose standards of
identity and composition are codified in Parts 319 and 381, subpart P.
The commenters noted that the wording in proposed 9 CFR 319.10(a) and
381.172(a) does not specifically include the standards described in the
Policy Book, while FSIS Policy Memo 123 does. They were concerned that
once the rule is in place, and Policy Memo 123 is rescinded, certain
products, such as ``Low Fat Pepperoni,'' would no longer be permitted
because pepperoni
[[Page 33805]]
does not have a standard of identity codified in the regulations.
Response: The policy embodied in the proposed general standard will
also apply to the informal standards for products, such as pepperoni,
that are described in the Policy Book. Thus, Policy Memo 121B and
Policy Memo 123 will not remain in effect once the proposed rule
becomes final. FSIS issued both Policy Memo 121B and Policy 123 as
interim measures to accommodate certain lower fat substitute meat and
poultry products until such time that rulemaking was completed. This
final rule incorporates, expands, and codifies the intent of these
policy memoranda. Thus, rescinding Policy Memo 121B and Policy Memo 123
will not preclude the production of products that have been made under
those policies. The Agency intends to clarify this point in a policy
bulletin, which is a more appropriate document for addressing the
informal standards described in the Policy Book.
Nutrient Content Claims That Emphasize the Presence of an Ingredient
Comment: Some commenters disagreed with the Agency's proposal to
permit only expressed nutrient content claims that relate to reductions
in constituents such as fat, cholesterol, or sodium, in conjunction
with the standardized name of the substitute product. These commenters
felt that nutrient content claims, such as ``high in'' and ``good
source of,'' that emphasize the presence of an ingredient, should also
be permitted to be used as part of the substitute standardized
product's name, provided that the product qualifies for these claims
under 9 CFR part 317 subpart B or 9 CFR 381 subpart Y.
Response: Under the current regulations, meat and poultry products
that satisfy the criteria for use of nutrient content claims defined in
9 CFR part 317 subpart B and 9 CFR 381 subpart Y are permitted to make
claims, such as ``high in'' or ``good source of,'' that emphasize the
presence of a nutrient. The ability to make these kinds of nutrient
content claims is not affected by this rulemaking.
In the preamble to the proposed rule, FSIS noted that the meat and
poultry product standards did not appear to preclude the making and
marketing of standardized products that qualify for the use of claims
such as ``high in'' and ``good source of.'' Therefore, in the proposed
regulation, the Agency did not expressly provide for these types of
nutrient content claims in the general standard. However, in the
proposal, FSIS did solicit comments on whether current regulatory
standards prevent the distribution of products with nutrient content
claims other than those that reflect a reduction in the level of a
nutrient.
None of the comments received suggested that the existing meat and
poultry product standards preclude the making and marketing of
standardized products that qualify for the use of claims such as ``high
in'' or ``good source of.'' Furthermore, because of the FSIS policy
that precludes direct nutrient fortification of meat and poultry
products, standardized meat and poultry products are not permitted to
be modified to qualify to use a nutrient content claim by adding
nutrients to the product. Therefore, FSIS has decided not to modify the
scope of coverage in this final rule to permit nutrient content claims
other than those that reflect a reduction of constituents that are of
health concern to some people, e.g., fat, cholesterol, and sodium, to
be used as part of the product name. Products that qualify for ``high
in'' and ``good source of'' nutrient content claims may continue to
highlight these claims as provided in 9 CFR 317.354 and 9 CFR 381.454.
Nutrient Fortification
Comment: Four commenters suggested that FSIS reexamine its policy
precluding direct nutrient fortification of meat and poultry products.
Two of these commenters suggested that FSIS allow selective nutrient
fortification in meat and poultry products to permit standardized
products to be modified so that they qualify to use nutrient content
claims, such as ``high in Vitamin A,'' as part of the product name. One
of these commenters requested that FSIS modify the language in proposed
9 CFR 319.10(a) to delete the following italicized words `` * * *
because of a compositional deviation that results from reduction of a
constituent that is described by an expressed nutrient content claim *
* *''
Another commenter suggested that FSIS permit selective protein
fortification in substitute standardize products so that they may use
claims such as ``High in Protein'' and ``Good Source of Protein'' as
part of the product name. This commenter recommended that FSIS continue
to require substitute standardized products to meet the same basic
minimum meat and poultry content requirements contained in the existing
meat and poultry product standards, but that the overall protein level
in these products should be allowed to be fortified using ingredients
such as soy protein. Another commenter that expressed support for
permitting direct nutrient fortification of meat and poultry products
felt that, because the over-consumption of protein in the American
diet, that protein fortification should not be permitted.
Two other commenters requested that FSIS allow fortification to
replace vitamins and minerals that may be lost due to formulation
adjustments to produce nutrient-modified foods. These commenters also
requested that FSIS exempt substitute standardized products subject to
the general standard from the minimum meat and poultry content
requirements imposed by the existing meat and poultry product
standards. Both commenters suggested that for these substitute
products, FSIS should focus on nutritional equivalency to the
traditional standardized product rather than meat content equivalency,
and permit reductions in the meat and poultry content for purposes of
reducing the product's fat content. The commenters stated that if FSIS
were to permit such reductions in the meat and poultry content,
fortification might be necessary to replace lost nutrients.
One commenter suggested that, while existing FDA regulations state
that the FDA does not consider it appropriate to fortify meat and
poultry products (21 CFR 104.20(a)), the FDA regulations appear to make
an exception for fortification of foods that replace traditional foods
when fortification is necessary to avoid nutritional inferiority.
Response: The comments requesting that FSIS reexamine its policy on
nutrient fortification raise some interesting points, particularly with
respect to the issues concerning nutritional equivalency versus meat
content equivalency. However, the decision to allow fortification of
meat and poultry products involves several complex issues, many of
which are outside the scope of this rulemaking.
FSIS'' fortification policy is derived from FDA's policy statement
on nutrient fortification codified at 21 CFR part 104, subpart B, which
states, in part, that the FDA ``* * * does not consider it appropriate
to fortify fresh produce; meat, poultry, or fish products * * * (21 CFR
104.20(a)). The fundamental objective of FDA's fortification policy is
``* * * to establish a uniform set of principles that will serve as a
model for the rational addition of nutrients to food'(21 CFR
104.20(a)). As stated in its policy, FDA determined that, ``* * *
random fortification of foods could result in over-or under-
fortification in consumer diets and create nutrient imbalances in the
food supply'' (21 CFR 104.20(a)).
[[Page 33806]]
FSIS has a long history of prohibiting direct fortification of meat
and poultry products, which is supported by the codified FDA
fortification policy. Thus, when determining whether to revise its
nutrient fortification policy for meat and poultry products, FSIS must
consider the issues in relationship to the codified FDA policy
statement on fortification. Furthermore, in order to maintain
consistent policies regarding nutrient fortification between the two
agencies, any effort by FSIS to revise its prohibition on direct
nutrient fortification of meat and poultry products should include FDA
participation and involve the scientific community (e.g., the National
Academy of Sciences, Institute of Medicine). FSIS, FDA, and the
scientific community need to first consider the guiding scientific
principles that form the basis for establishing a public health need
for fortifying meat and poultry with nutrients. Only after these
principles are applied could there be consideration of revising the
current fortification policy.\1\ Obviously, this type of effort is
outside the intended purpose and scope of this rulemaking. It would be
more appropriate to consider this matter in a separate rulemaking where
the Agency can receive the benefit of an open and thorough review of
all issues related to the fortification of meat and poultry products.
---------------------------------------------------------------------------
\1\ See report: Institute of Medicine, National Academy of
Science, 2003. Dietary Reference Intakes, Guiding Principles for
Nutrition Labeling and Fortification. The National Academies Press,
Washington, DC.
---------------------------------------------------------------------------
Furthermore, FSIS believes that the formulation adjustments needed
to produce substitute standardized products with reductions in
constituents such as fat, cholesterol, and sodium, will not result in a
product that is nutritionally inferior to the product for which it is a
substitute. Important nutrients, such as iron, zinc, B vitamins, and
protein, are associated with the lean muscle portion of meat and
poultry tissue, not the fat. Because the minimum meat and poultry
requirement for substitute standardized products is not changed by this
rule, reductions in the fat content should not affect the levels of
nutrients associated with the lean muscle portion of these products.
Therefore, nutrient fortification is not necessary to prevent the
products subject to the general standard defined by this rule from
being nutritionally inferior to the standardized products for which
they are a substitute.
Differences in Performance Characteristics
Comment: The proposed regulation stated that a substitute
standardized product with performance characteristics, e.g., cooking
quality, freezing quality, spreadability of product, and shelf-life,
that materially limit the use of the product must include a disclaimer
on the product's label adjacent to the product name informing the
consumer of such differences.
Most commenters agreed that limitations in a product's performance
characteristics should be disclosed on the product label, and be
conspicuous and readable. A number of commenters stated that the
disclaimer should be adjacent to the most prominent claim on the label.
One commenter, although in agreement with the disclaimer requirement,
felt that disclosure on the label, not necessarily adjacent to the
product name as provided in the proposed rule, was sufficient to inform
the consumer of performance differences. This same commenter
recommended that FSIS harmonize the requirement for labeling of
performance differences with a similar FDA rule, which requires a
disclaimer adjacent to the most prominent claim on the label (21 CFR,
101.13(d)). Another commenter stated that the disclaimer should be
adjacent to the most prominent claim and should most likely appear on
the principal display panel.
Response: In the preamble to the proposed rule, FSIS stated that
``if there is a difference in performance characteristics that
materially limits the use of the product, the product may still be
considered a substitute if the label includes a disclaimer adjacent to
the most prominent claim in accordance with 9 CFR 317.313(d)(1) and (2)
and 9 CFR 381.413(d)(1) and (2), informing the consumer of such
difference'' (60 FR 67480). However, in the text of the proposed rule,
FSIS stated that the label must include, ``adjacent to the product
name,'' a statement in accordance with 9 CFR 317.313(d)(1) and (2) and
9 CFR 381.413(d)(1) and (2) informing the consumer of differences in
performance characteristics (60 FR 67486, 67487). Thus, the preamble
and the text of the proposed rule differed in that the preamble did not
mention that the disclaimer must be ``adjacent to the product name.''
The regulations referenced by both the preamble and the text of the
proposed rule, 9 CFR 317.313(d)(1) and 9 CFR 381.413(d)(1), require
that differences in performance characteristics that materially limit
the performance of a substitute product be disclosed adjacent to the
most prominent claim on the product label.
FSIS is resolving the discrepancy regarding placement of the
disclaimer. FSIS agrees with the comment that disclosure on the label,
not necessarily adjacent to the product name, is sufficient to inform
the consumer of performance differences. Therefore, in this final rule,
FSIS is not requiring that the disclaimer be placed adjacent to the
product name. As in FDA regulations 21 CFR 130.10 and 101.13(d), a
disclaimer for differences in performance characteristics shall be
placed adjacent to the most prominent claim on the label. To reflect
this decision, FSIS is removing the phrase ``adjacent to the product
name'' from proposed Sec. Sec. 319.10(b)and 381.172(b).
Comment: Two commenters disagreed with the need for the proposed
disclaimer requirement and suggested that disclosure of any limitations
in the performance characteristics of a substitute standardized product
be voluntary. One of these commenters stated that disclaimers on a
product's labeling informing consumers of performance characteristics
that materially limit the use of the product need not be required by
regulations because a substitute standardized product produced under
the general standard will succeed or fail in the market place based on
consumer expectations associated with the product's performance. This
commenter stated that businesses would voluntarily place disclaimers on
a product's label in the absence of a regulation requiring that they do
so because it would be good business to inform consumers that a product
they are purchasing can not be used in a traditional application.
The other commenter agreed that, in practice, poorly formulated
products would fail in the marketplace long before any regulatory
system could determine that they did not meet the specific performance
characteristics they would be expected to have. However, this commenter
acknowledged that requiring a disclaimer informing consumers of
limitations in a product's performance characteristics, when they
exist, will require manufacturers of substitute standardized products
to monitor performance characteristics during product development and
may help ensure that new low- and reduced-fat standardized products are
formulated well from the beginning. The commenter went on to state that
consumers are also more likely to accept this category of substitute
products if they are well formulated from the beginning.
[[Page 33807]]
Response: FSIS disagrees with the commenters' suggestion that
disclosure of performance characteristics that materially limit the use
of a substitute standardized product compared to the use of the
traditional standardized product should be voluntary. The FMIA and the
PPIA require that the labeling of a meat or poultry product must be
truthful and not misleading, and that such labeling accurately disclose
to consumers what they are buying when they purchase any meat or
poultry product. Information disclosing differences in performance
characteristics that affect the use of a substitute standardized
product (e.g., cooking quality, freezing quality, spreadability of
product, and shelf life) is a material fact that must be disclosed on
the labeling of these products. Without such labeling, consumers would
be misled about significant characteristics and uses the product has
compared to the standardized product for which it substitutes.
Accordingly, this information must be communicated to consumers on the
product's label, or the label will be misleading and the product will
be misbranded under the FMIA or PPIA.
Moreover, FSIS agrees with the commenter who suggested that
processors are more likely to monitor the performance characteristics
of substitute standardized products during product development when
limitations in the product's performance characteristics are required
to be disclosed on the product's labeling. FSIS also agrees that if
substitute standardized products are well formulated from the
beginning, it will promote consumer acceptance of this category of meat
and poultry products.
Comment: One commenter pointed out that it may be possible for
performance characteristics to be introduced into a substitute
standardized product that improve upon the performance characteristics
of the traditional standardized product. The commenter suggested that
the Agency consider substituting the term ``not inferior'' for ``
similar'' in proposed 9 CFR 319.10(b).
Response: FSIS did not intend to prohibit improvements in the
performance characteristics of substitute products when it proposed
that substitute standardized products subject to the general standard
perform similarly to the traditional standardized products for which
they substitute. However, FSIS disagrees that it should require that
substitute standardized products have performance characteristics that
are ``not inferior to'' rather than ``similar to'' the traditional
standardized products as suggested by the commenter. As proposed,
Sec. Sec. 319.10(b) and 381.172(b) permit products subject to the
general standard to have limitations in performance characteristics
provided that such limitations are properly disclosed on the product's
labeling. The Agency believes that requiring disclosure of any
performance limitations on the labeling of products subject to the
general standard provides sufficient incentive for manufacturers of
these products to market products that are not inferior to the
traditional standardized products. Furthermore, proposed 9 CFR
319.10(b) and 9 CFR 381.172(b) require a disclaimer for performance
characteristics that ``materially limit'' the use of a substitute
standardized product, not for characteristics that improve the
performance of the product. Thus, the disclaimer requirement contained
in proposed 9 CFR 319.10(b) and 9 CFR 381.172(b) will not discourage
manufacturers from making improvements to the performance
characteristics of substitute products when it is possible to do so.
Enforcement
Comment: Two commenters questioned FSIS's ability to enforce and
ensure uniform compliance with the performance characteristics
requirements proposed in 9 CFR 319.10(b) and 381.172(b). One commenter
asked how FSIS intends to determine differences in performance
characteristics. The commenter went on to state that the proposed
performance characteristics requirements seem to be ``command and
control'' regulations that are not related to product safety. The other
commenter stated that, in practice, poorly formulated products would
fail in the marketplace long before any regulatory system could
determine that they did not meet the specific performance
characteristics discussed in the proposal.
Response: FSIS expects that substitute standardized products that
are produced under the general standard will conform to the performance
characteristics requirements set forth in proposed 9 CFR 319.10(b) and
381.172(b). To ensure that there is compliance, FSIS will examine the
performance characteristics and product quality of substitute products
as it would other types of products, through scientific review and
experimental investigations. In addition, FSIS will use traditional
methods available to the Agency, such as sample analysis, inspections,
surveys, and follow-up investigations of consumer and trade complaints
to identify products that do not comply with the new regulations in
order to enforce this regulation as the need arises.
Furthermore, FSIS disagrees with the comment that the proposed
performance characteristics requirements are ``command and control''
regulations. Under Sec. Sec. 319.10(b) and 381.172(b), FSIS is not
establishing specific criteria for determining similarities in
performance characteristics. FSIS believes that judgments about
similarity are best left to product developers, who have the incentive
to market a product that resembles the traditional standardized product
as closely as possible and to disclose product performance limitations
to ensure that there is consumer satisfaction with the substitute
standardized product.
Safe and Suitable Ingredients
Comment: There was general agreement among the commenters that the
ingredients used in a substitute standardized product produced under
the general standard should be those ingredients provided by the
traditional standard, with the exception of ``safe and suitable
ingredients,'' as defined in (former) 9 CFR 318.7 and 381.147, at the
minimum level necessary to improve texture and prevent syneresis.
However, several commenters requested clarification and expansion of
the ingredients permitted under this provision.
Three commenters stated that allowances for ingredients should be
broadened to include any safe and suitable ingredients to replace
functional characteristics. These commenters all noted that the FSIS
proposal limits ingredient usage to achieve textural improvement and to
prevent syneresis. They felt that FSIS should build additional
flexibility into the final rule to allow for a wider use of safe and
suitable ingredients to replace functional characteristics that may be
lost when a formulation is adjusted to meet a claim requirement. These
commenters mentioned that the comparable FDA regulation allows the use
of safe and suitable ingredients ``* * * to add flavor, extend shelf
life, improve appearance, or add sweetness'' (21 CFR 130.10(d)). One
commenter suggested that any ingredient that is generally recognized as
safe (GRAS) or that is an approved additive should be permitted to be
used as desired by the manufacturer. Another commenter stated that
limiting the use of safe and suitable ingredients to the minimum level
necessary to improve texture and to prevent syneresis severely limits
the ability to produce a consumer-acceptable meat or poultry product.
One
[[Page 33808]]
commenter specifically requested that FSIS clarify the acceptability of
flavorings, especially meat flavorings, as safe and suitable
ingredients in substitute standardized products.
Response: For purposes of clarification, since it published the
general standard proposal, FSIS issued the final rule ``Food
Ingredients and Sources of Radiation Listed or Approved for Use in Meat
and Poultry Products'' (64 FR 72168, December 23, 1999). The rule is
intended to improve the efficiency of the procedures used by FSIS and
FDA to review and approve the use of food ingredients and sources of
radiation in the production of meat and poultry products. Under the new
regulations, rather than listing substances approved for use in the
production of meat and poultry products in the chart of substances
contained in former 9 CFR 318.7(c)(4) and former 9 CFR 381.147(f)(4),
FDA now lists food ingredients and sources of radiation that are safe
for specific use in the production of meat and poultry products in its
regulations in title 21 of the CFR. In the final rule, FSIS also
created a list of food ingredients approved for use in the production
of meat and poultry products by combining the listing contained in
former section 318.7(c)(4) with the listing contained in former section
381.147(f)(4) and moving the combined listing to section 424.21(c). The
final rule became effective on January 24, 2000.
FSIS did not include ingredients that would affect flavor, shelf
life, or sweetness because these kinds of ingredients do not affect the
ability of a manufacturer to modify a meat or poultry product to reduce
fat, cholesterol, or sodium, which was the focus of this rulemaking.
Thus, Sec. Sec. 319.10 and 381.172 provide only for increased amounts
of safe and suitable ingredients that are needed to achieve the effect
of replacing fat, i.e., binders, texturizers, and emulsifiers.
As for the acceptability of flavorings in substitute standardized
products, manufacturers will not be limited by Sec. Sec. 319.10 or
381.172 in their ability to use ingredients that impart flavor. This
final rule does not limit a manufacturer's ability to use safe and
suitable meat and poultry flavorings.
``Fat Replacing'' Binders
Comment: In the preamble to the proposed rule, FSIS provided a list
of ``fat replacing'' binders to assist meat and poultry processors to
understand the types of ingredients that are permitted to be used to
achieve the effects of fat in making substitute standardized products
under the general standard. However, the list was not intended to be
all-inclusive. One commenter supported the use of ingredients not
identified in the preamble as part of a fat replacement system and
requested that FSIS clarify whether other fat replacers, such as milk
protein concentrates, would be permitted in substitute standardized
products, given this substance's similarities to the listed substances.
The commenter also requested that the preamble to the final rule
specifically note that milk protein concentrates and egg whites are
acceptable substances in fat replacement systems.
Three commenters agreed that the ingredients listed in the preamble
are appropriate for use in a substitute version of a standardized
product but felt that the list should be broadened to include other
safe and suitable ingredients that have a demonstrated ability to
function as a fat replacement system. One of these commenters requested
that if the list provided within the context of the preamble is not
meant to be all-inclusive, FSIS should state that fact. The commenters
also encouraged FSIS to include a list of criteria for evaluating fat
replacing binders not on the list to determine whether they qualify as
acceptable binders.
Response: The list of ``fat-replacing binders'' presented in the
preamble to the proposed rule represents examples of ingredients or
additives historically classified as binders by food scientists and
ingredient technologists. This list is not intended to be all
encompassing, and other safe and suitable ingredients historically
recognized as binders are permitted to be used in ``fat replacement''
systems for substitute standardized products produced under the general
standard.
In general, a safe and suitable ingredient qualifies for use as a
fat replacing binder under this final rule if it is only used for its
functional properties and does not impart other characterizing
qualities, such as taste and nutritional value, to the standardized
product when used in the product formulation. FSIS will evaluate
whether safe and suitable ingredients that were not listed in the
preamble to the proposal qualify as fat replacing ingredients on a
case-by-case basis.
As a point of clarification, milk protein concentrates have
historically been used by meat and poultry product manufacturers as
binding ingredients in meat and poultry products and therefore, under
the general standard, FSIS will permit milk protein concentrates to be
used as binders in fat replacement systems for substitute standardized
products.
Regarding the use of egg whites as a fat replacing binder, egg
whites are considered an egg product and as such function as an
individual food product that is consumed for its own taste and
nutritional value. Thus, FSIS considers the use of egg whites in the
formulation of a meat or poultry product to be sufficiently
characterizing so as to result in a product that is not a substitute
standardized product, but one that is a non-standardized product, e.g.,
identified with a true product name, such as ``Low Fat Pork Sausage
made with Egg Whites.''
Although FSIS is not providing an all inclusive list of suitable
fat replacing binders in this final rule, the Agency did provide an
extensive listing of binders in the preamble to the proposed rule to
convey the intent of the rule (see 60 FR 67481). Persons interested in
determining whether an ingredient is an appropriate fat replacing
binder may refer to this original listing.Furthermore, safe and
suitable ingredients that meet the general criteria outlined above,
i.e., have historically been classified as binders, are only used for
their functional properties, and do not impart other characterizing
qualities when used in the formulation of substitute products, will
also qualify as acceptable fat replacing binders under this final rule.
Textured Vegetable Protein (TVP) as a ``Fat Replacer''
Comment: In the preamble to the proposed rule, FSIS stated that the
Agency views TVP as a ``meat or poultry replacer,'' and that the use of
TVP as a fat replacing ingredient in a substitute standardized product
subject to the general standard would be inappropriate. At the time
that the proposal was published, FSIS had determined that the use of
TVP in a substitute standardized product would change the nature of the
product to such an extent that it would no longer be a substitute
product within the parameters of the proposed rule. This view, in part,
was based on the belief that TVP was used as a ``meat replacing''
ingredient in foods considered ``meat replacing products,'' such as
``veggie-burgers,'' which are primarily TVP with water, flavorings, and
seasonings.
FSIS received numerous comments expressing strong disagreement with
FSIS's historic views. Forty-three commenters submitted statements in
support of allowing TVP as a fat replacer in substitute standardized
meat and poultry products subject to the
[[Page 33809]]
general standard so that these products may be identified by a nutrient
content claim. Many of these commenters provided supporting studies on
the health and nutritional benefits of soy protein, along with data on
consumer awareness and acceptance of products containing TVP. Many
commenters felt that not permitting TVP as a fat replacing ingredient
would greatly limit the ability of the industry to develop substitute
standardized meat and poultry products that are lower in fat. These
commenters stated that the use of TVP as a fat replacer is important in
expanding the flexibility of the meat and poultry industry to create
and market an increased variety of healthful substitute meat and
poultry products. Some commenters specifically mentioned that
prohibiting TVP would limit product development in areas of coarse
ground cooked and fermented sausage.
Several commenters stated that TVP should be permitted as a fat
replacer so long as its use conforms to the requirements of the general
standard. These commenters stated that TVP should be permitted as part
of a ``fat replacement system'' in substitute standardized meat and
poultry products so long as: (1) Its use does not substantially change
the nature of the finished product; (2) it is not used to replace the
meat or poultry content required by the traditional standard; and (3)
it is used only at the minimum level necessary in a fat replacement
system to qualify for use of the nutrient content claim.
A number of commenters stated that TVP should be regulated on the
basis of its functional properties rather than on its physical form.
Many of these commenters pointed out that, while in the past TVP was
used as a ``filler'' or ``substitute'' for meat components in food,
advancements in TVP technology have made TVP a highly functional
ingredient that could now be used as part of a fat replacement system
to improve the textural character and quality of a substitute
standardized meat or poultry product. Many commenters noted that TVP,
when used in combination with other water binders, provides improved
product texture, visual appearance, performance, and storage
characteristics. Data supporting this view were presented to the
Agency.
Some commenters felt that TVP should be allowed as a fat replacer
in all meat items where non-textured vegetable proteins are allowed.
One commenter stated that texture is a matter of degree, and that forms
of vegetable proteins range from fine powders, to small granules, to
small flakes, to larger granules and flakes. This commenter stated that
it is arbitrary to require that TVP be excluded as a ``fat replacer''
but not the powdered forms. One commenter questioned the logic of
permitting soy flour, soy protein concentrate, and isolated soy protein
in products because they replace fat, but prohibiting the use of TVP
because it is inappropriately thought to replace meat. The commenter
pointed out that the proposed rule does not permit a reduction in the
meat or poultry content, and therefore, TVP could not be used as a meat
replacer. Another commenter mentioned that other binders, such as
carrageenan, can be texturized, and therefore, TVP is being singled out
unfairly.
A number of commenters stated that, because the presence of TVP can
be disclosed in product labeling, consumers should be allowed to decide
for themselves whether to purchase a lower fat standardized product
that contains TVP. Some commenters pointed out that the presence of TVP
in a meat food product could be communicated to consumers in the same
manner as any other ingredient, in the ingredient statement. The
commenters asserted that appropriate product labeling required by the
general standard would ensure that consumers would not be misled about
the presence of TVP in substitute standardized products produced.
Some commenters stated that if TVP is permitted as a fat replacer
in substitute standardized products, the substitute product should
provide the same amount of animal protein as the traditional
standardized product. One commenter stated that this approach would
provide manufacturers with optimum flexibility, yet guarantees that the
consumer receives a product that is at least as valuable as the
unmodified product. Another commenter mentioned that consumers are
interested in over-all nutrition, not in specific ingredients.
Some commenters expressed the view that TVP should not be
considered as a ``food,'' because it is not consumed by itself as a
food. These commenters stated that TVP is a functional food ingredient
that can be used as part of a fat replacement system.
Response: FSIS has been persuaded by the comments, information, and
other data submitted by commenters to permit the use of TVP as a part
of a fat replacing system in substitute standardize products produced
under the general standard. Accordingly, in this final rule, proposed
Sec. Sec. 319.10(c) and 381.172(c) have been modified to provide for
the use of TVP, alone or in combination with other binders and water,
as part of a fat replacement system.
The Agency will permit the use of TVP as a functional food
ingredient that is used to replace fat. Like the other fat replacing
ingredients permitted to be used under this final rule, the use of TVP
as an ingredient in a substitute standardized product will be permitted
only at the lowest level necessary to achieve the intended effect of
replacing fat. When TVP is used to replace fat, the ingredients
statement on the product label must alert the consumer to the fact that
TVP is not permitted in the traditional standardized product or is used
in excess of amounts permitted in the traditional standardized product.
The labeling requirements will ensure that consumers will not be misled
when TVP is used to replace fat in substitute standardized meat and
poultry products subject to the general standard.
Under this final rule, TVP may not be used to replace the meat or
poultry content of a product when a product standard specifies a
minimum meat or poultry content requirement. However, if the
formulation of a substitute product produced under the general standard
contains the same amount of meat or poultry prescribed by the
traditional standard, the fat component of the meat or poultry in the
substitute product may be removed during processing and replaced with
TVP, or any other safe and suitable binder, alone or in combination
with water as part of a fat replacement system.
For example, the product standard for ``chili con carne'' provides
that the product shall contain not less than 40% meat computed on the
weight of the fresh meat (9 CFR 319.300). The product formulation for a
substitute version of chili con carne produced under the general
standard must contain 40% meat, but the fat content of the meat
component may be replaced with TVP during processing.
According to information presented to the Agency, TVP is
particularly useful in developing lower fat versions of cooked sausages
and other comminuted meat and poultry products. Although the standards
for these kinds of products generally do not prescribe a minimum meat
or poultry content, most of these standards limit the amount of fat
that is permitted in the product. For example, the standard for cooked
sausages defined in 9 CFR 319.180 limits the fat content of these
products to no more than 30% of the finished product, and the standard
for ground beef defined in 9 CFR 319.15 limits the fat content in this
product to no more than 30%. Thus, under this final rule, the amount of
TVP permitted in such
[[Page 33810]]
products will be limited by both the requirement that fat replacing
ingredients may be used only at the lowest level necessary to replace
fat and by the minimum fat content requirement established by the
product standard.
For example, a substitute cooked sausage produced under the general
standard is permitted to contain up to 30% TVP, provided that the sole
function of the TVP is to replace the fat. For purposes of this rule,
FSIS does not consider replacing the fat component of a single
ingredient standardized product, such as ground beef, as reducing the
product's meat content, provided that the product complies with the
manufacturing and labeling requirements prescribed in this final rule.
To eliminate the possibility of confusion, the phrases ``textured
vegetable protein shall not replace meat'' and ``textured vegetable
protein shall not replace poultry,'' which were used as examples in the
regulatory text of proposed 9 CFR 319.10(c)(2) and 381.172(c)(2), will
be removed in the final rule. These phrases are unnecessary because the
regulation already prohibits reductions in the meat or poultry content
required by a regulatory standard regardless of whether TVP is used in
the product.
Other Foods as ``Fat Replacers''
Nine commenters indicated that in the final rule, FSIS should
permit foods, such as bread, rice, potatoes, fruits, and vegetables to
be used in substitute standardized meat and poultry products to reduce
their fat content. Some of these commenters stated that these
ingredients could serve the same role as the water and binder systems
permitted as fat replacers in the proposed rule, but that food
ingredients are more beneficial because they may contain some
nutritional constituents, such as vitamins and minerals, that many
binders do not. One commenter stated that food ingredients, when used
at proper levels, help to provide consumers with substitute
standardized products that perform similarly to traditional
standardized products. Another commenter stated that the nutrition
label would enable consumers to make informed purchase decisions based
on the entire nutritional profile of the product. This commenter
pointed out that many consumers would prefer the nutritional profile of
substitute standardized products that use starchy vegetables and
complex carbohydrates, such as rice and potatoes, rather than a
combination of water and ingredients such as highly refined vegetable
gums to lower the percentage of calories from fat. One commenter stated
that it makes sense to allow other foods as fat replacers if the goal
is to make more healthful products available to consumers. Another
commenter suggested that consumers might be more interested in overall
nutritional quality, taste, convenience, and performance of the product
than in the specific ingredients present in the product.
Response: FSIS concedes that because foods such as bread, rice,
potatoes, fruits, and vegetables, have little or no fat, their use as
ingredients in standardized meat and poultry product could have the
effect of reducing the fat content of such products. However, when
foods are used as ingredients in a standardized product, the
composition of the product may be altered to such an extent that the
resulting product is not a substitute version of the traditional
standardized product but a new and different product with a separate
identity that reflects the combination of the individual foods. For
example, because diced apples and rice are not specified as ingredients
in the standardized product ``Pork Sausage,'' when they are added to
``Pork Sausage,'' the result is a new product, which, provided that it
does not have a standard of identity or composition prescribed by 9 CFR
part 319 or other established common or usual name, is required to bear
a descriptive name, such as ``Pork Sausage with Diced Apples and
Rice,'' that clearly identifies the product (see 9 CFR 317.2(c)(1) and
(e) and 9 CFR 381.117(a)). Because the product ``Pork Sausage with
Diced Apples and Rice'' is a new product and not a substitute version
of the standardized product ``Pork Sausage,'' it is not the type of
product that the general standard established by this final rule is
intended to address.
As a point of clarification, this final rule does not prevent non-
standardized meat and poultry products that use food ingredients to
reduce their fat content from using a traditional nutrient content
claim permitted under 9 CFR 317 subpart B and 381 subpart Y, provided
they meet the requirements of the claim. For example, the product
``Pork Sausage with Diced Apples and Rice'' is permitted to bear the
claim ``low fat'' on its label if it complies with Sec. 317.362, and
therefore, may be referred to as ``Low Fat Pork Sausage with Diced
Apples and Rice.'' Consumers who prefer the nutritional profile of meat
and poultry products that use other foods, rather than binders and
water, or other functional food additives, to reduce their fat content
will be able to identify these products by their descriptive product
name and the traditional nutrient content claim on the product
labeling. Furthermore, any benefits in the nutritional profile of
products that use foods as ingredients to reduce their fat content will
be reflected in the nutrition facts panel, as well, if appropriate, in
other nutrient content claims.
Prohibited Ingredients
Comment: One commenter expressed agreement with the provision in
proposed 9 CFR 319.10(c)(3) and 381.172(c)(3) that states that
ingredients specifically prohibited for use in standardized meat and
poultry products should also be prohibited for use in substitute
standardized products subject to the general standard. However, the
commenter felt that ingredients prohibited from use in all meat and
poultry products should be based on safety considerations rather than
quality considerations.
Response: The general standard allows for the use of any safe and
suitable fat replacement ingredient, e.g., binders and water. Under the
Federal Food, Drug, and Cosmetic Act (21 U.S.C. 301 et seq.), FDA is
responsible for determining the safety of food ingredients for use in
food in general. Under the authority of the FMIA and PPIA, FSIS
acquiesces to FDA's safety judgments, but FSIS determines the
suitability of ingredients determined to be safe by FDA for use in meat
and poultry products. These responsibilities are fully described in the
final rule ``Food Ingredient and Sources of Radiation Listed or
Approved for Use in the Production of Meat and Poultry Products,''
which was published in the December 23, 1999, Federal Register (64 FR
72168).
Thus, although it is the responsibility of the FDA to evaluate the
safety of a substance for use in meat or poultry products, under the
authority of the FMIA and PPIA, FSIS may preclude the use of a
substance in meat or poultry products for reasons other than safety.
There are instances in which the use of a substance, even if safe, may
promote deception when used in a meat and poultry product, and,
accordingly, such use would be prohibited by FSIS. For example, paprika
is considered GRAS by FDA and is also listed for use as a color
additive, but the FSIS regulations prohibit its use on fresh, uncooked
meat products because such use adds color that may make the meat appear
fresher than it actually is (9 CFR 424.23(a)(1)). Therefore, it is
incumbent upon FSIS to consider suitability, as well as the safety, of
ingredients for use in the production of meat and poultry
[[Page 33811]]
products in order to prevent these products from being adulterated or
misbranded.
Processing Methods/Anatomical Location for Meat and Poultry Ingredients
Comment: One commenter stated that the provision in proposed
Sec. Sec. 319.10 and 381.172 that requires that the meat portion of a
substitute standardized product undergo the same basic processing
procedures as the traditional standardized product for which it is a
substitute has the potential to limit the use of new technologies
without producing any stated goal that would justify the limitation.
The commenter stated, that as long as the substitute standardized
product has performance characteristics that are similar to the
traditional standardized product, and is produced only from authorized
ingredients, additional restrictions on processing procedures are
unnecessary and undesirable.
Another commenter stated that the general standard should permit
substitute standardized products to contain different meat species and
different kinds of poultry than those prescribed by the traditional
standard, and that it should permit meat or poultry from different
anatomical locations than the locations prescribed by the traditional
standard, provided that the difference in species or anatomical
location is stated in the product name. This commenter felt that a
literal reading of the proposed regulation could be interpreted to mean
that products such as ``Beef Bacon'' or ``Pork Shoulder Bacon'' would
no longer be permitted to include the term ``Bacon'' in their product
names if coupled with a nutrient content claim. The commenter went on
to say that these kinds of products should continue to be permitted to
be marketed under the same familiar names that have been used in the
past, and that use of a nutrient content claim next to the product name
should not change this.
Response: The intent of the general standard for substitute
standardized products is to enable the meat and poultry industries to
produce modified versions of standardized products that have reductions
of certain constituents that are of health concern to some consumers,
such as fat, cholesterol, and sodium, and to increase flexibility and
support product innovation. Under this rule, deviations from the
existing standards are not expected to result in a product that no
longer resembles the original standardized product. Thus, the use of a
different meat species or kind of poultry, or the use of meat or
poultry from different anatomic locations from those specified in the
standard, that results in a product that is so physically dissimilar
from the traditional standardized product that it does not meet the
definition of ``substitute'' set forth in 9 CFR 317.313(d) and
381.413(d) would be inconsistent with the intent of this rule. For
these kinds of products to represent themselves as substitute
standardized products would be false and misleading under the FMIA and
PPIA.
As an illustration, the regulatory standard for ``Bacon'' under 9
CFR 319.107 requires that this product be prepared from cured, sliced
pork bellies. Curing and slicing a cut of meat from a different
livestock species or from a different anatomical location, or preparing
sliced pork bellies using a method other than curing, would result in a
product with physical characteristics so different from the
standardized product ``Bacon'' that the resulting product could not be
considered a ``substitute'' for bacon under 9 CFR 317.313(d) and
381.413(d). Thus, instead of being identified as a substitute product,
the product would be identified by a descriptive term such as ``Beef
Bacon'' or ``Pork Shoulder Bacon.''
However, FSIS will consider the types of changes requested by the
commenters, such as amending a standard to permit the use of
alternative processing methods, on a case-by-case basis. FSIS agrees
that certain technologies used to prepare standardized foods may yield
a product with the same physical, nutritional, and sensory
characteristics as the food made in accordance with the traditional
standards. To reflect this fact, instead of specifying that substitute
standardized products must contain all ingredients specifically
required by a standard of identity or composition, and that the meat or
poultry portion of substitute products come from the same anatomical
location, be of the same kind and amount, and undergo the same basic
processing procedures as the standardized product as was proposed, FSIS
is revising Sec. Sec. 319.10(c)(4) and 381.172(c)(4) to require only
that substitute standardized products comply with all other applicable
standards of identity or composition.
Regarding the comment expressing concern that under the general
standard, products such as ``Beef Bacon'' or ``Pork Shoulder Bacon''
would no longer be permitted to include ``Bacon'' in their product
names if coupled with a nutrient content claim, as previously
mentioned, FSIS intends to apply the principles embodied in the general
standard established by this final rule to other products as
appropriate. The Agency will clarify this fact in a policy bulletin
after this final rule is published.
Thus, this final regulation will not prohibit the ``bacon-like''
products described in the Policy Book, such as ``Turkey Bacon-Cured
Turkey Breast Meat-Chopped and Formed,'' from being modified to qualify
to use a nutrient content claim as part of the product name. The
modified version of this ``bacon-like'' product would be permitted to
be identified as ``Low Fat Turkey Bacon-Cured Turkey Breast Meat-
Chopped and Formed.'' FSIS reiterates that the intent of this rule is
to provide a wider array of nutritionally improved substitute products
that would provide consumers with more meat and poultry products from
which to choose. The intent is not to diminish or interfere with
markets providing innovative as well as traditional kinds of products
to consumers.
Minimum Meat and Poultry Requirement
Comment: Several commenters submitted statements both for and
against the proposed requirement that a substitute standardized product
subject to the general standard rule maintain the same minimum meat or
poultry requirement as the standardized product for which it is a
substitute. Seven commenters agreed that substitute standardized
products should be required to maintain the minimum meat and poultry
requirement established by the traditional standard, while ten
commenters expressed disagreement with this requirement.
Several commenters stated that the meat or poultry content of a
standardized product often contains the highest concentration of fat,
and, while it may be theoretically possible for manufacturers to use
leaner meat to reduce fat, it is not economical. One of these
commenters stated that fat-reduced products that meet the existing
minimum meat or poultry content requirement would be prohibitively
expensive. Another commenter stated that relying exclusively on leaner
meat to reduce fat might also make products tougher in texture and less
palatable. Another commenter stated that, without reducing the ``meat
block'' (meat or poultry content), the proposed general standard can
not deliver on its promise to encourage innovation and the production
of nutritionally improved meat and poultry products.
Some commenters stated that minimum meat and poultry content
requirements for substitute products are not necessary so long as the
labeling of
[[Page 33812]]
the substitute standardized products provides sufficient information to
distinguish these products from the traditional standardized products
for which they substitute. One commenter submitted data showing that
consumers do not mind if part of the meat block in a substitute product
is replaced with another ingredient, so long as the labeling of the
substitute standardized product discloses the presence of the replacing
ingredient. Another commenter stated that trends in consumer behavior,
which include reducing the amount of meat consumed in order to reduce
fat intake, strongly support the argument that consumers will not be
misled by nutrient-modified food products that contain less meat and
poultry than is required by the traditional standardized form of the
food. One commenter suggested that a substitute standardized product
with reductions in its meat or poultry content should state on its
label that, ``in order to reduce fat, this product contains less meat
than the traditional standardized product.'' Some commenters stated
that nutritional equivalency, rather than meat-content equivalency,
should serve as the basis for defining requirements for the use of
nutrient content claims. These commenters felt that FSIS should allow
for necessary reductions in meat or poultry content to meet the
requirements of the claim, with the reduction accomplished in such a
manner that nutritional equivalency to the traditional standardized
product is maintained. One commenter stated that meat replacers may be
more desirable than some of the fat replacers, which hold water but
contribute little in taste or nutritional value.
One commenter stated that it is widely recognized that the
requirements for minimum meat content are based on the notion that meat
and poultry represented the most valuable constituent of a meat or
poultry product. This commenter claimed that meat and poultry are
simply no longer the indisputable ``highest value'' components of food
products. Another commenter mentioned that FDA regulations provide for
marketing of products, such as reduced-fat peanut butter, which allows
for reduction of the peanut content of the product below that required
for the standardized product.
Those commenters that agreed with the requirement that substitute
standardized products subject to the general standard maintain the same
minimum meat and poultry requirement as the standardized product for
which they are a substitute maintained that consumers have come to
expect a certain amount of meat or poultry in products that bear a
standardized term, and that the meat and poultry content of the product
is still the most valued constituent.
Response: Because many consumers have come to expect a certain
amount of meat or poultry in products that bear a standardized term,
deviations in the prescribed meat or poultry content will not be
permitted in this final rule. Moreover, while FSIS appreciates these
comments, the Agency does not view this rulemaking as the appropriate
vehicle for changing the specific meat and poultry content requirements
of meat and poultry product standards. These issues will be considered
in a separate rulemaking that will examine FSIS's overall regulatory
approach to standardized meat and poultry products that was described
in the ANPR ``Meat and Poultry Standards of Identity and Composition''
published in the September 9, 1996, edition of the Federal Register (61
FR 47453).
In response to that ANPR, FSIS and FDA are jointly working on a
more comprehensive approach to modernizing food standards whose goal is
to establish ``general principles'' that interested parties could
follow in requesting changes to food standards. One change that
interested parties may be able to pursue, if these principles are
adopted, would be reductions in the meat or poultry content
requirements of stand