Shiga Toxin-Producing Escherichia coli (STEC) in Certain Raw Beef Products, 68843-68846 [2014-27418]
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Federal Register / Vol. 79, No. 223 / Wednesday, November 19, 2014 / Notices
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Done at Washington, DC, on November 14,
2014.
Mary Frances Lowe,
U.S. Manager for Codex Alimentarius.
[FR Doc. 2014–27413 Filed 11–18–14; 8:45 am]
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DEPARTMENT OF AGRICULTURE
Food Safety and Inspection Service
[Docket No. FSIS–2010–0023]
Shiga Toxin-Producing Escherichia
coli (STEC) in Certain Raw Beef
Products
Food Safety and Inspection
Service, USDA.
ACTION: Notice of availability and
response to comments.
AGENCY:
The Food Safety and
Inspection Service (FSIS) is announcing
that it has completed and is making
available its analysis on the estimated
costs and benefits associated with the
implementation of its non-O157 STEC
testing on beef manufacturing trimmings
and the costs and benefits associated
with the potential expansion of its nonO157 STEC testing to ground beef and
ground beef components other than beef
manufacturing trimmings. In addition,
FSIS is responding to comments that it
received on the previous cost benefits
analysis.
SUMMARY:
To receive full consideration,
comments should be received by
January 20, 2015.
ADDRESSES: FSIS invites interested
persons to submit comments on this
notice and the cost benefit analysis.
Comments may be submitted by one of
the following methods:
• Federal eRulemaking Portal: This
Web site provides the ability to type
short comments directly into the
comment field on this Web page or
attach a file for lengthier comments. Go
to https://www.regulations.gov. Follow
the on-line instructions at that site for
submitting comments.
• Mail, including CD–ROMs: Send to
Docket Clerk, U.S. Department of
Agriculture, Food Safety and Inspection
Service, Patriots Plaza 3, 1400
Independence Avenue SW., Mailstop
3782, Room 8–163A, Washington, DC
20250–3700.
• Hand- or courier-delivered
submittals: Deliver to Patriots Plaza 3,
355 E Street SW., Room 8–163A,
Washington, DC 20250–3700.
Instructions: All items submitted by
mail or electronic mail must include the
Agency name and docket number FSIS
2010–0023. Comments received in
response to this docket will be made
available for public inspection and
posted without change, including any
personal information, to https://
www.regulations.gov.
Docket: For access to background
documents or comments received, go to
the FSIS Docket Room at Patriot Plaza
DATES:
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68843
3, 355 E Street SW., Room 8–164,
Washington, DC 20250–3700 between
8:00 a.m. and 4:30 p.m., Monday
through Friday.
FOR FURTHER INFORMATION CONTACT:
Daniel L. Engeljohn, Ph.D., Assistant
Administrator, Office of Policy and
Program Development, Food Safety and
Inspection Service, U.S. Department of
Agriculture; Telephone: (202) 205–0495.
SUPPLEMENTARY INFORMATION:
Background
On September 20, 2011, FSIS
announced in the Federal Register its
determination that raw, non-intact beef
products or raw, intact beef products
that are intended for use in raw, nonintact product, that are contaminated
with Shiga toxin-producing Escherichia
coli (STEC) O26, O45, O103, O111,
O121, or O145 are adulterated within
the meaning of 21 U.S.C. 601(m)(1)(76
FR 58157; Sep. 20, 2011). In support of
its determination, the Agency cited
evidence of the STEC organisms’ high
pathogenicity, low infectious dose,
transmissibility from person to person,
and thermal resistance high enough for
them to survive ordinary cooking (76 FR
51858–51859). FSIS stated that raw,
non-intact beef products that are
contaminated with these STEC are also
unhealthful and unwholesome (under
21 U.S.C. 601(m)(3)) (76 FR 58159).
In this 2011 Federal Register notice,
FSIS included an estimate of costs and
benefits of testing for non-O157 STEC in
all non-intact beef product subject to
Agency testing (76 FR 58157; Sept. 20,
2011, at 58162–58164). The Agency
asked for comments on its plans for
implementing the program, including
cost estimates (76 FR 58164), which
included costs to FSIS laboratories for
analyzing trim samples for non-O157
STEC (approximately $204,050 to
$338,270 per year in 2010 dollars), cost
of additional establishments testing for
non-O157 (about $12.3 million to $16.4
million per year), and the loss to the
industry from diverting the
contaminated products (about $12.1 to
$16.1 million per year). FSIS also
announced in this notice its plan to
conduct a new ‘‘checklist’’ survey of its
field inspection personnel who are
stationed in beef slaughter and
processing establishments.
FSIS implemented a verification
sampling and testing program for the six
adulterant non-O157 STEC in raw beef
manufacturing trimmings on June 4,
2012, as announced in a 2012 Federal
Register notice (77 FR 9889; Feb. 2012).
The Agency also announced (75 FR
31975 at 31976; May 31, 2012) that it
would update and revise the September
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20, 2011, economic analysis, respond to
comments received on the analysis, and
assess the economic effects of testing for
the specified STECs on raw beef
manufacturing trimmings, other raw
ground beef components, and ground
beef. FSIS also announced that when
the economic analysis was complete,
the Agency would announce its
availability, request comments on it,
assess the comments, and make any
necessary changes to the analysis before
finalizing the analysis and expanding
FSIS testing to include other raw ground
beef components and ground product.
Summary of the Economic Analysis
FSIS has estimated the cost to the
regulated industry and FSIS associated
with the implementation of its nonO157 STEC testing on beef
manufacturing trimmings since June
2012, based on Agency testing data and
information collected through the FSIS
2013 Pathogen Controls in Beef
Operations Survey. This survey is
available at: [https://www.fsis.usda.gov/
wps/wcm/connect/184a3baa-2f73-46518aba-68124580f4e0/Pathogen_Controls_
in_Beef_Operations_Survey.pdf?MOD=
AJPERES. The survey report is at:
[https://www.fsis.usda.gov/wps/wcm/
connect/6d37a1fc-a3e1-40b6-90cc719bdb391522/STEC_Survey_
Comments_Summary.pdf?MOD=
AJPERES], and the cost-benefit analysis
is at: [https://www.fsis.usda.gov/wps/
portal/fsis/topics/regulations/federalregister/federal-register-notices]. The
cost for the current testing of beef
manufacturing trimmings (including
Agency and the industry testing) is
about $1.37 million. If the Agency
expands the testing to bench trim, other
components, and raw ground beef, it
will add another $1 million to the cost
and bring up the grand total to about
$2.37 million. Of the $2.37 million,
$1.38 million is for FSIS and $0.99
million for the industry.
FSIS also assessed the benefits
associated with the new testing. Benefits
would accrue from reduced illnesses
and deaths, reduced outbreak-related
recalls, and improved business
practices. FSIS has concluded that the
benefits accruing to industry,
Government, and consumers from this
new testing policy will result in net
economic benefits. However, FSIS was
not able to quantify the benefits of
expanding the testing.
Summary of the New Checklist Survey
Results
In May–July 2013, FSIS conducted the
checklist survey entitled, ‘‘The Pathogen
Controls in Beef Operations Survey.’’
The purpose of the survey was to gather
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information on the controls that beef
slaughtering and processing
establishments have in place to reduce
STEC and Salmonella contamination.
The survey questions covered a wide
range of topics, including establishment
pre-harvest management controls,
establishment sanitary dressing
procedures, establishment carcass
sampling and testing, establishment use
of high event periods, information on
which beef products are produced at
particular establishments, and controls
that establishments use to address
STEC. FSIS sent surveys to inspectors in
486 establishments out of a total of
approximately 2,300 beef slaughter or
beef processing establishments to collect
the information. The survey results
related to non-O157 STEC testing
include that about 29 percent of the beef
establishments reassessed their HACCP
plans for raw beef products based on
FSIS’s new non-O157 STEC policy, and
about 43 percent of the establishments
that tested for non-O157 STEC took
more than one action (such as
confirmatory testing following
presumptive positive results or cooking)
with products that screened positive.
FSIS used the survey results and an
updated risk assessment to develop the
updated economic analysis.
Response to Comments on the 2011
Federal Register Notice
Comment: A trade association stated
that the FSIS verification sampling and
testing for non-O157 STEC will lead to
additional costs for taxpayers and
consumers because of increased testing
and destruction or diversion of meat.
Response: FSIS recognizes that FSIS
testing will likely result in additional
costs to establishments. The Agency
understands that the industry is likely
to transfer some of its costs to
consumers. The Agency has determined,
however, that the benefits resulting from
reduced illness and deaths, reduced
outbreak-related recalls, and improved
business practices justify the costs.
Comment: A trade association stated
that FSIS underestimated the cost to the
Agency and to the industry of
implementing this new program.
According to the commenter, the true
cost of Agency testing, including the
cost for testing ground beef, would total
$1,170,564 per year in additional
expenses. The commenter also stated
that adding the costs attendant on a
‘‘for-cause Food Safety Assessment,’’
which FSIS conducts when ground beef
is confirmed to contain STEC, would
add an additional $854,000. According
to the comment, FSIS has grossly
underestimated the cost of
implementing this policy testing.
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Response: The Agency has updated
the cost estimate to include the costs of
expanding testing to raw ground beef
products and other raw ground beef
components (other than manufacturing
trimmings). FSIS found that there will
be additional benefits, as well as
additional costs, should the Agency
begin testing additional product for nonO157 STEC. As mentioned in the
Summary of Economic Analysis, the
cost for the current testing of beef
manufacturing trimmings (including
Agency and the industry testing) is
about $1.37 million. If the Agency
expands the testing to bench trim, other
components, and raw ground beef, it
will add another $1 million to the cost
and bring the grand total to about $2.37
million. Of the $2.37 million, $1.38 is
for FSIS and $0.99 for the industry.
FSIS also estimated the benefits
associated with the new testing policy.
Benefits would accrue from reduced
illnesses and deaths, reduced outbreakrelated recalls, and improved business
practices. The Agency still concludes
that the costs are low for new testing
that is warranted, and that the benefits
justify the costs.
Comment: A trade association stated
that the Agency grossly miscalculated
the costs to industry and made seriously
flawed assumptions in its cost analysis
when it concluded that only 33 percent
of beef slaughter establishments test for
E. coli O157:H7. The trade association
stated that the better measure for this
analysis would be to use the data in
Table 5.2.10 in FSIS’ 2007 checklist
study—‘‘Testing of Source Materials for
03B Establishments.’’
Response: The Agency has updated
the cost analysis adopting a slightly
different approach with information
from our 2013 Pathogen Controls in Beef
Operations Survey. Thus, there is no
reason to use the outdated data from the
2007 checklist study any more. Details
are in the updated cost-benefit analysis.
Comment: A trade association stated
that FSIS estimated in the 2011 Federal
Register notice that approximately 20
percent of establishments were testing
for non-O157 STEC and did not
adequately support that estimate. The
comment further stated that the Agency
failed to account properly for added
laboratory costs for the industry. The
commenter stated that industry analysis
estimates added laboratory costs to the
industry to range from $2.5 million to
almost $2.9 million annually.
Response: The Agency has updated
the cost analysis using information from
the 2013 Pathogen Controls in Beef
Operations Survey and used a slightly
different approach from the approach
used in the earlier estimate. This
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approach is based on the number of
samples tested by the industry and
accounts for the added laboratory costs
as well. The commenter did not provide
information on how the laboratory costs
of $2.5 million to $2.9 million were
derived. As is explained in the revised
cost benefit analysis, FSIS estimates that
these costs to industry would be $0.99
million, and these costs to FSIS would
be $1.38 million.
Comment: A trade association
commented that the Agency’s estimate
of total beef trimmings production—
2.05 billion pounds—is inaccurate. The
trade association claimed that, for the
year ending June 30, 2010, the industry
produced 6.96 billion pounds of ground
beef, and that, since ground beef is only
produced from raw ground beef
components, i.e., trimmings, the more
realistic volume of beef trimmings is
also approximately 6.96 billion pounds.
Additionally, the trade association
stated that because the amount of
trimmings is approximately 3.4 times
greater than the Agency estimate, a more
accurate range of the cost of diverted
products is approximately $13.24
million to $17.65 million dollars. A
foreign government stated that the value
of product that is confirmed positive
and diverted for cooking will be
reduced by approximately 70 to 75
percent.
Response: The Agency has updated
the cost analysis and does not use
estimated production volume or the
value lost for products diverted for
cooking in the updated analysis. In
examining the 2013 Pathogen Controls
in Beef Operations Survey data, we
found that 43 percent of the
establishments that tested for non-O157
STEC took more than one action,
including proceeding to confirmation
testing, cooking, destroying, and others,
with products that screened positive.
The Agency believes that it is not
possible to get the total volume of the
products disposed under any of the
actions, even if we asked that question,
because the actions the establishments
choose are often based on their
particular circumstances. For example,
if the establishment is very confident
with its screening test methodology, it
will probably cook the products that
screen positive subject to available
cooking capacity. If the establishment is
not confident about its screening
methodology, and there is not enough
cooking capacity, it will probably
proceed to confirmation or destroy the
products, depending on the relative
costs of conducting confirming tests
versus destroying the products.
Empirical literature on industry
behavior shows that industry behaves
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strategically to maximize profits or
minimize losses.
Therefore, establishments’ choice of
action with regard to product that
screened positive will be based on
particular circumstances, and whatever
actions an establishment takes, the
incentive is to avoid recalls and
potential outbreaks at the minimum
cost. Furthermore, if industry focused
more on using the data from the
verification testing conducted by the
establishment and FSIS to improve the
prevention efforts at slaughter, there
would be even less contaminated
product to be diverted.
Comment: Several industry
commenters stated that the Agency
improperly calculates the cost of
holding tested product and fails to
consider the additional time needed to
complete the STEC test through the final
stage of confirmation and the other costs
attendant thereto.
Response: If industry decides to hold
product that screened positive in their
own testing until confirmed positive
results are attained, then this is a
business decision not driven by FSIS.
Today, establishments do not typically
await a confirmed positive result before
taking action on the affected production
lot. Industry responds to the screen
positive result, as stated by another
commenter below. The new non-O157
STEC screen method that FSIS uses
takes the same amount of time as the
method for E. coli O157:H7. Agency
data for FY2013 showed that the screen
positive sample rate for non-O157 STEC
in beef manufacturing trimming is only
2 percent. Therefore, the additional cost
of holding products because of
additional FSIS testing and additional
positive samples is likely to be minimal.
Comment: A trade association
representing the meat industry stated
that there will be more recalls based on
testing, and that the Agency’s economic
analysis failed to consider recalls. The
industry, however, estimates that the
new testing will result in at least 24
additional recalls annually and perhaps
as many as 48 additional recalls.
According to the commenter, using
Agency data, those added recalls will
cost the industry between $72 million
and $144 million annually.
Response: For FSIS testing, the
establishments have to hold products
that screened positive, and therefore
there should be no recalls. Recalls
should only happen when
establishments failed to hold positive
products from their own testing. Since
FSIS started testing in June 2012, there
have been only two Class-I recalls
associated with raw beef products with
non-O157 STEC, and in both cases
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products were recalled before any
illness was reported. These early-stage
recalls actually carried the benefit of
preventing potential outbreaks and
outbreak-related recalls, which are more
costly to the industry as well as the
consumers and the government. The
goal of the new policy is to better ensure
that adulterated product does not enter
commerce and, hence, will not have to
be recalled.
Comment: A trade association
representing the meat industry
suggested that there will be significant
impact on a significant number of small
and very small businesses from
increased cost of raw materials, holding
tested product, resources needed for
supporting documentation, validation,
and verification that current control
programs for O157 are effective against
the six additional STEC strains, and
from reassessing HACCP plans.
Response: Any increase in the cost of
raw materials would be borne by large
establishments as well. The Agency
believes that the increased cost from
holding the tested product because of
additional testing and additional
positive samples will not be significant
because Agency test data for FY 2013
showed that the screen positive sample
rate for non-O157 STEC in beef
manufacturing trimming is only 2
percent. The cost of documentation and
reassessment of HACCP plans will be
minimal too, as the small and very small
businesses have to reassess their HACCP
plans at least annually. Again, a focus
on preventing contamination is likely to
be more effective than reliance on
testing.
Comment: A trade association
representing the meat industry has
estimated that the cost per test is $19,
plus an additional $9 if the sample is a
presumptive positive during the screen.
An estimate for final confirmatory
testing was not completed by the
commenter, as the commenter noted
that the beef industry generally makes
disposition decisions based upon
potential positive results.
Response: The cost per test is more
complicated than just one dollar figure.
There are many methodologies available
to the industry, and some
establishments use different
methodologies for different time-periods
(such as high-prevalence season and
other time-periods). For those
establishments that are already testing
for E. coli O157:H7, adding non-O157
will, in most cases, involve switching to
new test kits. Market information and
Agency expert opinion indicate that the
new test kits will only cost about $1 or
$2 more per test. If an establishment has
to contract out to a different laboratory
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for non-O157 STEC analysis, we used
$30 for average cost per test based on
the cost of FSIS testing methodology,
which is available in the market for the
industry.
Comment: Some countries exporting
beef that commented have estimated the
direct cost increase to be around $2.4
million per annum for new non-O157
STEC testing. Three commenters from
Australia stated that the costs will be
significant; two of them said that the
cost of testing, storage, and
documentation could amount to AUD
1.8 million per annum. One commenter
from another country stated that having
to test United States-destined trimmings
for non-O157 STEC as well as for E. coli
O157:H7 would impose an additional
multi-million dollar cost burden.
Response: FSIS does not require
foreign establishments to test, just as we
did not require domestic establishments
to test. The foreign establishments, as
well as the U.S. establishments, have
many alternatives to control for nonO157 STECs. It is the foreign
establishments’ business decision as to
what control measure(s) will be the
most cost-effective for them to adopt.
FSIS testing policy does not create any
unfair burden on the foreign
establishments.
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USDA Nondiscrimination Statement
The U.S. Department of Agriculture
(USDA) prohibits discrimination in all
its programs and activities on the basis
of race, color, national origin, gender,
religion, age, disability, political beliefs,
sexual orientation, and marital or family
status. (Not all prohibited bases apply to
all programs.) Persons with disabilities
who require alternative means for
communication of program information
(Braille, large print, audiotape, etc.)
should contact USDA’s Target Center at
202–720–2600 (voice and TTY).
To file a written complaint of
discrimination, write USDA, Office of
the Assistant Secretary for Civil Rights,
1400 Independence Avenue SW.,
Washington, DC 20250–9410 or call
202–720–5964 (voice and TTY). USDA
is an equal opportunity provider and
employer.
Additional Public Notification
Public awareness of all segments of
rulemaking and policy development is
important. Consequently, FSIS will
announce it on-line through the FSIS
Web page located at: https://www.fsis.
usda.gov/federal-register.
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,
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regulations, Federal Register notices,
FSIS public meetings, and other types of
information that could affect or would
be of interest to our constituents and
stakeholders. The Update is available on
the FSIS Web page. Through 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 automatic and
customized access to selected food
safety news and information. This
service is available at https://www.fsis.
usda.gov/subscribe. Options range from
recalls, export information, regulations,
directives, and notices. Customers can
add or delete subscriptions themselves,
and have the option to password protect
their accounts.
Done, at Washington, DC, November 14,
2014.
Alfred V. Almanza,
Acting Administrator.
[FR Doc. 2014–27418 Filed 11–18–14; 8:45 am]
BILLING CODE 3410–DM–P
DEPARTMENT OF AGRICULTURE
National Institute of Food and
Agriculture
Solicitation of Veterinary Shortage
Situation Nominations for the
Veterinary Medicine Loan Repayment
Program (VMLRP)
National Institute of Food and
Agriculture, United States Department
of Agriculture (USDA).
AGENCY:
Notice and solicitation for
nominations.
ACTION:
The National Institute of Food
and Agriculture (NIFA) is soliciting
nominations of veterinary service
shortage situations for the Veterinary
Medicine Loan Repayment Program
(VMLRP) for fiscal year (FY) 2015, as
authorized under the National
Veterinary Medical Services Act
(NVMSA), 7 U.S.C. 3151a. This notice
initiates a 60-day nomination period
and prescribes the procedures and
criteria to be used by State, Insular Area,
DC and Federal Lands to nominate
veterinary shortage situations. Each year
all eligible nominating entities may
submit nominations, up to the
maximum indicated for each entity in
this notice. NIFA is conducting this
solicitation of veterinary shortage
situation nominations under a
previously approved information
collection (OMB Control Number 0524–
0046).
SUMMARY:
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Shortage situation nominations,
both new and carry over, must be
submitted on or before January 20, 2015.
ADDRESSES: Submissions must be made
by email at vmlrp@nifa.usda.gov to the
Veterinary Medicine Loan Repayment
Program; National Institute of Food and
Agriculture; U.S. Department of
Agriculture.
FOR FURTHER INFORMATION CONTACT: Gary
Sherman; National Program Leader,
Veterinary Science; National Institute of
Food and Agriculture; U.S. Department
of Agriculture; STOP 2220; 1400
Independence Avenue SW.,
Washington, DC 20250–2220; Voice:
202–401–4952; Fax: 202–401–6156;
Email: vmlrp@nifa.usda.gov.
SUPPLEMENTARY INFORMATION:
DATES:
Background and Purpose
A series of three peer-reviewed
studies published in 2007 in the Journal
of the American Veterinary Medical
Association (JAVMA), and sponsored by
the Food Supply Veterinary Medicine
Coalition (www.avma.org/KB/
Resources/Reference/Pages/about-fsvmcoalition.aspx), drew considerable
attention to an existing and apparent
growing shortage of food supply
veterinarians, the causes of shortages in
this sector, and the consequences to the
U.S. food safety infrastructure and to the
general public if this trend continues to
worsen. Subsequently the Government
Accountability Office released a report
entitled ‘‘Veterinary Workforce: Actions
Are Needed to Ensure Sufficient
Capacity for Protecting Public and
Animal Health’’ (GAO–09–178: Feb 18,
2009). This report was followed by a
National Academies of Science report in
2013 entitled ‘‘Workforce needs in
Veterinary Medicine’’. While the 2013
report concluded that some sectors of
the veterinary workforce are not in
shortage, the authors affirmed that
‘‘livestock farmers who live far from
populated areas have difficulty
obtaining veterinary care.’’ Furthermore,
regarding the largest subgroup of
veterinarians serving the food animal
industries, the reported stated, ‘‘. . .
new graduates are not entering this type
of practice anymore, [and therefore]
food-animal-predominant veterinarians,
as a group, are now composed of
rapidly-aging members.’’
Food supply veterinary medicine
embraces a broad array of veterinary
professional activities, specialties and
responsibilities, and is defined as the
full range of veterinary medical
practices contributing to the production
of a safe and wholesome food supply
and to animal, human, and
environmental health. The privately
E:\FR\FM\19NON1.SGM
19NON1
Agencies
[Federal Register Volume 79, Number 223 (Wednesday, November 19, 2014)]
[Notices]
[Pages 68843-68846]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2014-27418]
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DEPARTMENT OF AGRICULTURE
Food Safety and Inspection Service
[Docket No. FSIS-2010-0023]
Shiga Toxin-Producing Escherichia coli (STEC) in Certain Raw Beef
Products
AGENCY: Food Safety and Inspection Service, USDA.
ACTION: Notice of availability and response to comments.
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SUMMARY: The Food Safety and Inspection Service (FSIS) is announcing
that it has completed and is making available its analysis on the
estimated costs and benefits associated with the implementation of its
non-O157 STEC testing on beef manufacturing trimmings and the costs and
benefits associated with the potential expansion of its non-O157 STEC
testing to ground beef and ground beef components other than beef
manufacturing trimmings. In addition, FSIS is responding to comments
that it received on the previous cost benefits analysis.
DATES: To receive full consideration, comments should be received by
January 20, 2015.
ADDRESSES: FSIS invites interested persons to submit comments on this
notice and the cost benefit analysis. Comments may be submitted by one
of the following methods:
Federal eRulemaking Portal: This Web site provides the
ability to type short comments directly into the comment field on this
Web page or attach a file for lengthier comments. Go to https://www.regulations.gov. Follow the on-line instructions at that site for
submitting comments.
Mail, including CD-ROMs: Send to Docket Clerk, U.S.
Department of Agriculture, Food Safety and Inspection Service, Patriots
Plaza 3, 1400 Independence Avenue SW., Mailstop 3782, Room 8-163A,
Washington, DC 20250-3700.
Hand- or courier-delivered submittals: Deliver to Patriots
Plaza 3, 355 E Street SW., Room 8-163A, Washington, DC 20250-3700.
Instructions: All items submitted by mail or electronic mail must
include the Agency name and docket number FSIS 2010-0023. Comments
received in response to this docket will be made available for public
inspection and posted without change, including any personal
information, to https://www.regulations.gov.
Docket: For access to background documents or comments received, go
to the FSIS Docket Room at Patriot Plaza 3, 355 E Street SW., Room 8-
164, Washington, DC 20250-3700 between 8:00 a.m. and 4:30 p.m., Monday
through Friday.
FOR FURTHER INFORMATION CONTACT: Daniel L. Engeljohn, Ph.D., Assistant
Administrator, Office of Policy and Program Development, Food Safety
and Inspection Service, U.S. Department of Agriculture; Telephone:
(202) 205-0495.
SUPPLEMENTARY INFORMATION:
Background
On September 20, 2011, FSIS announced in the Federal Register its
determination that raw, non-intact beef products or raw, intact beef
products that are intended for use in raw, non-intact product, that are
contaminated with Shiga toxin-producing Escherichia coli (STEC) O26,
O45, O103, O111, O121, or O145 are adulterated within the meaning of 21
U.S.C. 601(m)(1)(76 FR 58157; Sep. 20, 2011). In support of its
determination, the Agency cited evidence of the STEC organisms' high
pathogenicity, low infectious dose, transmissibility from person to
person, and thermal resistance high enough for them to survive ordinary
cooking (76 FR 51858-51859). FSIS stated that raw, non-intact beef
products that are contaminated with these STEC are also unhealthful and
unwholesome (under 21 U.S.C. 601(m)(3)) (76 FR 58159).
In this 2011 Federal Register notice, FSIS included an estimate of
costs and benefits of testing for non-O157 STEC in all non-intact beef
product subject to Agency testing (76 FR 58157; Sept. 20, 2011, at
58162-58164). The Agency asked for comments on its plans for
implementing the program, including cost estimates (76 FR 58164), which
included costs to FSIS laboratories for analyzing trim samples for non-
O157 STEC (approximately $204,050 to $338,270 per year in 2010
dollars), cost of additional establishments testing for non-O157 (about
$12.3 million to $16.4 million per year), and the loss to the industry
from diverting the contaminated products (about $12.1 to $16.1 million
per year). FSIS also announced in this notice its plan to conduct a new
``checklist'' survey of its field inspection personnel who are
stationed in beef slaughter and processing establishments.
FSIS implemented a verification sampling and testing program for
the six adulterant non-O157 STEC in raw beef manufacturing trimmings on
June 4, 2012, as announced in a 2012 Federal Register notice (77 FR
9889; Feb. 2012). The Agency also announced (75 FR 31975 at 31976; May
31, 2012) that it would update and revise the September
[[Page 68844]]
20, 2011, economic analysis, respond to comments received on the
analysis, and assess the economic effects of testing for the specified
STECs on raw beef manufacturing trimmings, other raw ground beef
components, and ground beef. FSIS also announced that when the economic
analysis was complete, the Agency would announce its availability,
request comments on it, assess the comments, and make any necessary
changes to the analysis before finalizing the analysis and expanding
FSIS testing to include other raw ground beef components and ground
product.
Summary of the Economic Analysis
FSIS has estimated the cost to the regulated industry and FSIS
associated with the implementation of its non-O157 STEC testing on beef
manufacturing trimmings since June 2012, based on Agency testing data
and information collected through the FSIS 2013 Pathogen Controls in
Beef Operations Survey. This survey is available at: [https://www.fsis.usda.gov/wps/wcm/connect/184a3baa-2f73-4651-8aba-68124580f4e0/Pathogen_Controls_in_Beef_Operations_Survey.pdf?MOD=AJPERES. The survey
report is at: [https://www.fsis.usda.gov/wps/wcm/connect/6d37a1fc-a3e1-40b6-90cc-719bdb391522/STEC_Survey_Comments_Summary.pdf?MOD=AJPERES],
and the cost-benefit analysis is at: [https://www.fsis.usda.gov/wps/portal/fsis/topics/regulations/federal-register/federal-register-notices]. The cost for the current testing of beef manufacturing
trimmings (including Agency and the industry testing) is about $1.37
million. If the Agency expands the testing to bench trim, other
components, and raw ground beef, it will add another $1 million to the
cost and bring up the grand total to about $2.37 million. Of the $2.37
million, $1.38 million is for FSIS and $0.99 million for the industry.
FSIS also assessed the benefits associated with the new testing.
Benefits would accrue from reduced illnesses and deaths, reduced
outbreak-related recalls, and improved business practices. FSIS has
concluded that the benefits accruing to industry, Government, and
consumers from this new testing policy will result in net economic
benefits. However, FSIS was not able to quantify the benefits of
expanding the testing.
Summary of the New Checklist Survey Results
In May-July 2013, FSIS conducted the checklist survey entitled,
``The Pathogen Controls in Beef Operations Survey.'' The purpose of the
survey was to gather information on the controls that beef slaughtering
and processing establishments have in place to reduce STEC and
Salmonella contamination. The survey questions covered a wide range of
topics, including establishment pre-harvest management controls,
establishment sanitary dressing procedures, establishment carcass
sampling and testing, establishment use of high event periods,
information on which beef products are produced at particular
establishments, and controls that establishments use to address STEC.
FSIS sent surveys to inspectors in 486 establishments out of a total of
approximately 2,300 beef slaughter or beef processing establishments to
collect the information. The survey results related to non-O157 STEC
testing include that about 29 percent of the beef establishments
reassessed their HACCP plans for raw beef products based on FSIS's new
non-O157 STEC policy, and about 43 percent of the establishments that
tested for non-O157 STEC took more than one action (such as
confirmatory testing following presumptive positive results or cooking)
with products that screened positive. FSIS used the survey results and
an updated risk assessment to develop the updated economic analysis.
Response to Comments on the 2011 Federal Register Notice
Comment: A trade association stated that the FSIS verification
sampling and testing for non-O157 STEC will lead to additional costs
for taxpayers and consumers because of increased testing and
destruction or diversion of meat.
Response: FSIS recognizes that FSIS testing will likely result in
additional costs to establishments. The Agency understands that the
industry is likely to transfer some of its costs to consumers. The
Agency has determined, however, that the benefits resulting from
reduced illness and deaths, reduced outbreak-related recalls, and
improved business practices justify the costs.
Comment: A trade association stated that FSIS underestimated the
cost to the Agency and to the industry of implementing this new
program. According to the commenter, the true cost of Agency testing,
including the cost for testing ground beef, would total $1,170,564 per
year in additional expenses. The commenter also stated that adding the
costs attendant on a ``for-cause Food Safety Assessment,'' which FSIS
conducts when ground beef is confirmed to contain STEC, would add an
additional $854,000. According to the comment, FSIS has grossly
underestimated the cost of implementing this policy testing.
Response: The Agency has updated the cost estimate to include the
costs of expanding testing to raw ground beef products and other raw
ground beef components (other than manufacturing trimmings). FSIS found
that there will be additional benefits, as well as additional costs,
should the Agency begin testing additional product for non-O157 STEC.
As mentioned in the Summary of Economic Analysis, the cost for the
current testing of beef manufacturing trimmings (including Agency and
the industry testing) is about $1.37 million. If the Agency expands the
testing to bench trim, other components, and raw ground beef, it will
add another $1 million to the cost and bring the grand total to about
$2.37 million. Of the $2.37 million, $1.38 is for FSIS and $0.99 for
the industry.
FSIS also estimated the benefits associated with the new testing
policy. Benefits would accrue from reduced illnesses and deaths,
reduced outbreak-related recalls, and improved business practices. The
Agency still concludes that the costs are low for new testing that is
warranted, and that the benefits justify the costs.
Comment: A trade association stated that the Agency grossly
miscalculated the costs to industry and made seriously flawed
assumptions in its cost analysis when it concluded that only 33 percent
of beef slaughter establishments test for E. coli O157:H7. The trade
association stated that the better measure for this analysis would be
to use the data in Table 5.2.10 in FSIS' 2007 checklist study--
``Testing of Source Materials for 03B Establishments.''
Response: The Agency has updated the cost analysis adopting a
slightly different approach with information from our 2013 Pathogen
Controls in Beef Operations Survey. Thus, there is no reason to use the
outdated data from the 2007 checklist study any more. Details are in
the updated cost-benefit analysis.
Comment: A trade association stated that FSIS estimated in the 2011
Federal Register notice that approximately 20 percent of establishments
were testing for non-O157 STEC and did not adequately support that
estimate. The comment further stated that the Agency failed to account
properly for added laboratory costs for the industry. The commenter
stated that industry analysis estimates added laboratory costs to the
industry to range from $2.5 million to almost $2.9 million annually.
Response: The Agency has updated the cost analysis using
information from the 2013 Pathogen Controls in Beef Operations Survey
and used a slightly different approach from the approach used in the
earlier estimate. This
[[Page 68845]]
approach is based on the number of samples tested by the industry and
accounts for the added laboratory costs as well. The commenter did not
provide information on how the laboratory costs of $2.5 million to $2.9
million were derived. As is explained in the revised cost benefit
analysis, FSIS estimates that these costs to industry would be $0.99
million, and these costs to FSIS would be $1.38 million.
Comment: A trade association commented that the Agency's estimate
of total beef trimmings production--2.05 billion pounds--is inaccurate.
The trade association claimed that, for the year ending June 30, 2010,
the industry produced 6.96 billion pounds of ground beef, and that,
since ground beef is only produced from raw ground beef components,
i.e., trimmings, the more realistic volume of beef trimmings is also
approximately 6.96 billion pounds. Additionally, the trade association
stated that because the amount of trimmings is approximately 3.4 times
greater than the Agency estimate, a more accurate range of the cost of
diverted products is approximately $13.24 million to $17.65 million
dollars. A foreign government stated that the value of product that is
confirmed positive and diverted for cooking will be reduced by
approximately 70 to 75 percent.
Response: The Agency has updated the cost analysis and does not use
estimated production volume or the value lost for products diverted for
cooking in the updated analysis. In examining the 2013 Pathogen
Controls in Beef Operations Survey data, we found that 43 percent of
the establishments that tested for non-O157 STEC took more than one
action, including proceeding to confirmation testing, cooking,
destroying, and others, with products that screened positive. The
Agency believes that it is not possible to get the total volume of the
products disposed under any of the actions, even if we asked that
question, because the actions the establishments choose are often based
on their particular circumstances. For example, if the establishment is
very confident with its screening test methodology, it will probably
cook the products that screen positive subject to available cooking
capacity. If the establishment is not confident about its screening
methodology, and there is not enough cooking capacity, it will probably
proceed to confirmation or destroy the products, depending on the
relative costs of conducting confirming tests versus destroying the
products. Empirical literature on industry behavior shows that industry
behaves strategically to maximize profits or minimize losses.
Therefore, establishments' choice of action with regard to product
that screened positive will be based on particular circumstances, and
whatever actions an establishment takes, the incentive is to avoid
recalls and potential outbreaks at the minimum cost. Furthermore, if
industry focused more on using the data from the verification testing
conducted by the establishment and FSIS to improve the prevention
efforts at slaughter, there would be even less contaminated product to
be diverted.
Comment: Several industry commenters stated that the Agency
improperly calculates the cost of holding tested product and fails to
consider the additional time needed to complete the STEC test through
the final stage of confirmation and the other costs attendant thereto.
Response: If industry decides to hold product that screened
positive in their own testing until confirmed positive results are
attained, then this is a business decision not driven by FSIS. Today,
establishments do not typically await a confirmed positive result
before taking action on the affected production lot. Industry responds
to the screen positive result, as stated by another commenter below.
The new non-O157 STEC screen method that FSIS uses takes the same
amount of time as the method for E. coli O157:H7. Agency data for
FY2013 showed that the screen positive sample rate for non-O157 STEC in
beef manufacturing trimming is only 2 percent. Therefore, the
additional cost of holding products because of additional FSIS testing
and additional positive samples is likely to be minimal.
Comment: A trade association representing the meat industry stated
that there will be more recalls based on testing, and that the Agency's
economic analysis failed to consider recalls. The industry, however,
estimates that the new testing will result in at least 24 additional
recalls annually and perhaps as many as 48 additional recalls.
According to the commenter, using Agency data, those added recalls will
cost the industry between $72 million and $144 million annually.
Response: For FSIS testing, the establishments have to hold
products that screened positive, and therefore there should be no
recalls. Recalls should only happen when establishments failed to hold
positive products from their own testing. Since FSIS started testing in
June 2012, there have been only two Class-I recalls associated with raw
beef products with non-O157 STEC, and in both cases products were
recalled before any illness was reported. These early-stage recalls
actually carried the benefit of preventing potential outbreaks and
outbreak-related recalls, which are more costly to the industry as well
as the consumers and the government. The goal of the new policy is to
better ensure that adulterated product does not enter commerce and,
hence, will not have to be recalled.
Comment: A trade association representing the meat industry
suggested that there will be significant impact on a significant number
of small and very small businesses from increased cost of raw
materials, holding tested product, resources needed for supporting
documentation, validation, and verification that current control
programs for O157 are effective against the six additional STEC
strains, and from reassessing HACCP plans.
Response: Any increase in the cost of raw materials would be borne
by large establishments as well. The Agency believes that the increased
cost from holding the tested product because of additional testing and
additional positive samples will not be significant because Agency test
data for FY 2013 showed that the screen positive sample rate for non-
O157 STEC in beef manufacturing trimming is only 2 percent. The cost of
documentation and reassessment of HACCP plans will be minimal too, as
the small and very small businesses have to reassess their HACCP plans
at least annually. Again, a focus on preventing contamination is likely
to be more effective than reliance on testing.
Comment: A trade association representing the meat industry has
estimated that the cost per test is $19, plus an additional $9 if the
sample is a presumptive positive during the screen. An estimate for
final confirmatory testing was not completed by the commenter, as the
commenter noted that the beef industry generally makes disposition
decisions based upon potential positive results.
Response: The cost per test is more complicated than just one
dollar figure. There are many methodologies available to the industry,
and some establishments use different methodologies for different time-
periods (such as high-prevalence season and other time-periods). For
those establishments that are already testing for E. coli O157:H7,
adding non-O157 will, in most cases, involve switching to new test
kits. Market information and Agency expert opinion indicate that the
new test kits will only cost about $1 or $2 more per test. If an
establishment has to contract out to a different laboratory
[[Page 68846]]
for non-O157 STEC analysis, we used $30 for average cost per test based
on the cost of FSIS testing methodology, which is available in the
market for the industry.
Comment: Some countries exporting beef that commented have
estimated the direct cost increase to be around $2.4 million per annum
for new non-O157 STEC testing. Three commenters from Australia stated
that the costs will be significant; two of them said that the cost of
testing, storage, and documentation could amount to AUD 1.8 million per
annum. One commenter from another country stated that having to test
United States-destined trimmings for non-O157 STEC as well as for E.
coli O157:H7 would impose an additional multi-million dollar cost
burden.
Response: FSIS does not require foreign establishments to test,
just as we did not require domestic establishments to test. The foreign
establishments, as well as the U.S. establishments, have many
alternatives to control for non-O157 STECs. It is the foreign
establishments' business decision as to what control measure(s) will be
the most cost-effective for them to adopt. FSIS testing policy does not
create any unfair burden on the foreign establishments.
USDA Nondiscrimination Statement
The U.S. Department of Agriculture (USDA) prohibits discrimination
in all its programs and activities on the basis of race, color,
national origin, gender, religion, age, disability, political beliefs,
sexual orientation, and marital or family status. (Not all prohibited
bases apply to all programs.) Persons with disabilities who require
alternative means for communication of program information (Braille,
large print, audiotape, etc.) should contact USDA's Target Center at
202-720-2600 (voice and TTY).
To file a written complaint of discrimination, write USDA, Office
of the Assistant Secretary for Civil Rights, 1400 Independence Avenue
SW., Washington, DC 20250-9410 or call 202-720-5964 (voice and TTY).
USDA is an equal opportunity provider and employer.
Additional Public Notification
Public awareness of all segments of rulemaking and policy
development is important. Consequently, FSIS will announce it on-line
through the FSIS Web page located at: https://www.fsis.usda.gov/federal-register.
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, and other types of information
that could affect or would be of interest to our constituents and
stakeholders. The Update is available on the FSIS Web page. Through 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 automatic and customized access to selected food
safety news and information. This service is available at https://www.fsis.usda.gov/subscribe. Options range from recalls, export
information, regulations, directives, and notices. Customers can add or
delete subscriptions themselves, and have the option to password
protect their accounts.
Done, at Washington, DC, November 14, 2014.
Alfred V. Almanza,
Acting Administrator.
[FR Doc. 2014-27418 Filed 11-18-14; 8:45 am]
BILLING CODE 3410-DM-P