Standards for the Growing, Harvesting, Packing, and Holding of Produce for Human Consumption; Extension of Compliance Dates for Subpart E, 9706-9714 [2019-04652]
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DEPARTMENT OF HEALTH AND
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Food and Drug Administration
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21 CFR Part 112
RIN 0910–AH93
Standards for the Growing, Harvesting,
Packing, and Holding of Produce for
Human Consumption; Extension of
Compliance Dates for Subpart E
Food and Drug Administration,
HHS.
ACTION:
FOR FURTHER INFORMATION CONTACT:
Samir Assar, Center for Food Safety and
Applied Nutrition (HFS–317), Food and
Drug Administration, 5001 Campus Dr.,
College Park, MD 20740, 240–402–1636.
SUPPLEMENTARY INFORMATION:
Table of Contents
I. Executive Summary
II. Background
III. Analysis and Response to Public
Comments
IV. Economic Analysis of Impacts
V. Analysis of Environmental Impact
VI. Paperwork Reduction Act of 1995
VII. Federalism
VIII. Consultation and Coordination With
Indian Tribal Governments
IX. References
I. Executive Summary
[Docket No. FDA–2011–N–0921]
AGENCY:
produce other than sprouts, are delayed
to January 26, 2024, for very small
businesses, January 26, 2023, for small
businesses, and January 26, 2022, for all
other businesses.
Final rule.
SUMMARY: The Food and Drug
Administration (FDA, the Agency, or
we) is extending, for covered produce
other than sprouts, the dates for
compliance with the agricultural water
provisions in the ‘‘Standards for the
Growing, Harvesting, Packing, and
Holding of Produce for Human
Consumption’’ rule. We are extending
the compliance dates to address
questions about the practical
implementation of compliance with
certain provisions and to consider how
we might further reduce the regulatory
burden or increase flexibility while
continuing to protect public health.
DATES: As of March 18, 2019 the
compliance dates for the agricultural
water provisions (subpart E) in the
Standards for the ‘‘Growing, Harvesting,
Packing, and Holding of Produce for
Human Consumption’’ rule (November
27, 2015, 80 FR 74354), for covered
The final rule extends, for covered
produce other than sprouts, the dates for
compliance with the agricultural water
provisions in the ‘‘Standards for the
Growing, Harvesting, Packing, and
Holding of Produce for Human
Consumption’’ rule. The agricultural
water provisions are contained in
subpart E of that rule. We are also
simplifying the compliance date
structure under subpart E as applied to
non-sprout covered produce, while
retaining date-staggering based on size.
The new compliance dates for the
agricultural water requirements in
subpart E for non-sprout covered
produce are January 26, 2024, for very
small businesses; January 26, 2023, for
small businesses; and January 26, 2022,
for all other businesses.
The final rule does not alter the
requirements in subpart E and therefore
the estimated costs and benefits accrued
in any given year of compliance with
the produce safety regulation, relative to
the first year of compliance, do not
change. However, because the
compliance dates for the agricultural
water provisions are extended, the
discounted value of both total costs and
total benefits decrease.
The impact of this final rule is
summarized in the following table.
TABLE 1—SUMMARY OF CHANGES TO BENEFITS AND COSTS AS A RESULT OF THE FINAL RULE
Units
Primary
estimate
Category
Year dollars
Forgone Benefits:
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Discount rate
(%)
Period
covered
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TABLE 1—SUMMARY OF CHANGES TO BENEFITS AND COSTS AS A RESULT OF THE FINAL RULE—Continued
Units
Primary
estimate
Category
Annualized ................................................................................................
Monetized $millions/year ..........................................................................
Forgone Costs:
Annualized ................................................................................................
Monetized $millions/year ..........................................................................
II. Background
This extension of compliance dates
concerns one of the seven foundational
rules that we have established in Title
21 of the Code of Federal Regulations
(21 CFR), Part 112 as part of our
implementation of the FDA Food Safety
Modernization Act (FSMA; Pub. L. 111–
353): ‘‘Standards for the Growing,
Harvesting, Packing, and Holding of
Produce for Human Consumption’’ (the
produce safety regulation, published in
the Federal Register of November 27,
2015, 80 FR 74354) (https://
www.fda.gov/fsma). We proposed this
extension in a proposed rule published
on September 13, 2017 (82 FR 42963).
We have reviewed the comments
submitted in response to the proposed
rule, and we respond to those comments
in section II. In this final rule we are
extending the compliance dates as
proposed.
In the preamble of the final rule
establishing the produce safety
regulation, we stated that the produce
Year dollars
Discount rate
(%)
Period
covered
$96
104
2017
2017
7
3
2016–2025
2016–2025
10
12
2017
2017
7
3
2016–2025
2016–2025
safety regulation would be effective on
January 26, 2016, and provided for
compliance dates of 1 to 6 years from
the effective date depending on farm
size, commodity, and provision(s) (see
table entitled ‘‘compliance dates’’ in the
preamble of the final rule establishing
the produce safety regulation, 80 FR
74354 at 74357, as corrected in a
technical amendment at 81 FR 26466,
May 3, 2016). (Some of the compliance
dates identified in the technical
amendment fall on weekends (i.e.,
January 26, 2019, is a Saturday and
January 26, 2020, is a Sunday) and
should therefore be read as referring to
the next business day (i.e., January 28,
2019, and January 27, 2020,
respectively). We use the latter dates
throughout this document.)
For the majority of agricultural water
provisions at subpart E (and for most of
the other provisions in the rule), with
respect to covered produce other than
sprouts, we provided compliance
periods of 4 years from the effective date
of the rule for very small businesses, 3
years for small businesses, and 2 years
for all other businesses.1 We provided
an additional 2 years beyond those
compliance periods for certain water
quality requirements in § 112.44 and
related provisions in §§ 112.45 and
112.46. See table 2.
In a final rule, ‘‘The Food and Drug
Administration Food Safety
Modernization Act; Extension and
Clarification of Compliance Dates for
Certain Provisions of Four
Implementing Rules’’ (81 FR 57784,
August 24, 2016) we also extended the
compliance date for certain ‘‘customer
provisions’’ in four of the seven
foundational rules that we have
established as part of our
implementation of FSMA, including the
produce safety regulation (§ 112.2(b)(3)).
In that final rule, we also clarified how
we interpret the compliance dates for
certain agricultural water testing
provisions established in the produce
safety regulation.
TABLE 2—AS STATED IN PRODUCE SAFETY REGULATION, COMPLIANCE DATES FOR REQUIREMENTS IN SUBPART E (AGRICULTURAL WATER) FOR COVERED ACTIVITIES INVOLVING COVERED PRODUCE (EXCEPT SPROUTS SUBJECT TO SUBPART M)
Compliance dates of 2–4 years applicable to the
farm based on its size
Extended compliance date of additional 2 years beyond the
compliance date based on size of farm
§ 112.41.
§ 112.42.
§ 112.43.
§ 112.45(b).
§ 112.45(a) with respect to safe and adequate standard.
§ 112.46(a).
§ 112.46(b)(1) with respect to untreated surface water.
§ 112.47.
§ 112.48.
§ 112.49.
§ 112.50.
§ 112.44.
§ 112.45(a) with respect to § 112.44(a) criterion.
§ 112.46(b)(1) with respect to untreated ground water.
§ 112.46(b)(2) and (b)(3).
§ 112.46(c).
FDA has received feedback from
numerous stakeholders raising issues
regarding the practicality of some of the
agricultural water requirements in the
produce safety regulation as applied to
covered produce other than sprouts.
Many of these concerns relate to the
testing requirements for pre-harvest
agricultural water, which are different
for sprouts than they are for other types
of covered produce. We are extending
these compliance dates in light of the
feedback we have received. Additional
time allows us to consider how to
approach these issues.
1 Under the produce safety regulation, a farm is
a very small business if, on a rolling basis, the
average annual monetary value of produce it sold
during the previous 3-year period is no more than
$250,000. A farm is a small business if, on a rolling
basis, the average annual monetary value of
produce it sold during the previous 3-year period
is no more than $500,000; and the farm is not a very
small business. See 21 CFR 112.3.
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As part of this extension, we are
simplifying the subpart E compliance
period structure such that all the
compliance dates for subpart E
provisions as applied to non-sprout
covered produce will occur at the same
time, retaining date-staggering based on
farm size. Accordingly, covered farms
will have 2 years beyond the previously
published compliance dates for the
water quality requirements in § 112.44
and related provisions in §§ 112.45 and
112.46, to comply with all of subpart E.
Put another way, we are extending the
compliance dates for provisions in the
first column of table 2 by 4 years and
extending the compliance dates for
provisions in the second column of
table 2 by 2 years, so that the
compliance dates for non-sprout
covered produce for all provisions of
subpart E are those listed in table 3.
TABLE 3—COMPLIANCE DATES FOR REQUIREMENTS IN SUBPART E FOR COVERED ACTIVITIES INVOLVING COVERED
PRODUCE (EXCEPT SPROUTS SUBJECT TO SUBPART M)
Time periods starting from the effective date
of the November 27, 2015, produce safety
final rule (January 26, 2016)
Size of covered farm
Compliance period
Very Small Business ........................................................................................................................
Small Business ................................................................................................................................
All Other Businesses .......................................................................................................................
This rule is limited in scope to
extending the compliance dates for
covered produce other than sprouts. The
rule does not address the underlying
requirements in subpart E, but only the
compliance dates for those requirements
(for covered produce other than
sprouts).
We conducted a qualitative
assessment of risk of hazards associated
with produce production during the
produce safety rulemaking, which
indicates that agricultural water is a
potential route of contamination of
produce during growing, harvesting,
and on-farm postharvest activities and
that use of poor agricultural practices
could lead to contamination and illness
even where the potential for
contamination is relatively low. We
remain firmly committed to sciencebased minimum standards directed to
agricultural water to minimize the risk
of serious adverse health consequences
or death from the use of, or exposure to,
covered produce, including those
reasonably necessary to prevent the
introduction of known or reasonably
foreseeable hazards into covered
produce, and to provide reasonable
assurances that the produce is not
adulterated under section 402 of the
Federal Food, Drug, and Cosmetic Act
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(FD&C Act) (21 U.S.C. 342). To that end,
we have been pursuing and will
continue to pursue a rigorous
stakeholder engagement plan in the
coming months as we consider the
practical implementation of the
agricultural water requirements and
how to best achieve these important
public health objectives. Along with
farmers and others in the produce
industry, in February 2018 we
participated in a summit at which
participants proposed and discussed
potential approaches to addressing
concerns with the existing agricultural
water requirements. We are also
continuing visits to farms throughout
the country to further refine our
understanding of the myriad variations
in agricultural water sources and uses.
We will continue to consult with
experts in produce safety, water
systems, and water microbiology, from
both the public and private sectors, to
take advantage of the very latest
scientific developments and
conclusions, particularly around water
quality criteria, sampling, and testing.
This rule does not change the
compliance dates for sprouts. In the
final produce safety regulation, we
provided staggered compliance periods
based on farm size for covered activities
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8 years ......................
7 years ......................
6 years ......................
Compliance date
January 26, 2024.
January 26, 2023.
January 26, 2022.
involving sprouts. The compliance date
for activities involving sprouts for very
small businesses is January 28, 2019.
The compliance date for activities
involving sprouts for small businesses is
January 26, 2018. The compliance date
for activities involving sprouts for all
other businesses is January 26, 2017.
The final produce safety regulation
established sprout-specific requirements
on multiple topics, including
agricultural water. The agricultural
water requirements for sprouts are
different from the agricultural water
requirements for other produce
commodities (compare §§ 112.44(a)(1)
and 112.44(b)). We have not received
any significant feedback from sprout
farms that subpart E has posed
particular challenges. Accordingly, as
proposed, we are not taking action with
regard to compliance dates for activities
involving sprouts.
Table 4 summarizes the compliance
dates for the produce safety regulation
based on this final rule. Time periods
start from the effective date of the
produce safety rule (January 26, 2016)
except as otherwise specified.
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III. Analysis and Response to Public
Comments
In response to the proposed rule, we
received comments from covered farms,
consumer protection groups, groups
representing these stakeholders, and
state governments. Many of the
comments were supportive of the
proposed extension and simplification
of compliance dates. In this final rule,
we respond to comments related to
whether FDA should extend the
compliance dates and simplify the
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compliance date structure for the
agricultural water requirements for
covered produce other than sprouts. We
did not consider and do not address
comments that raised issues beyond the
narrow scope of the proposed rule,
including comments related to
withdrawal or modifications to subpart
E or comments related to broader policy
issues. FDA will take these additional
comments into consideration as we
consider approaches to address
agricultural water requirements. In this
final rule we also do not address
specific questions on the produce safety
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9709
regulation, but the Technical Assistance
Network remains an available resource
for such questions (https://www.fda.gov/
food/guidanceregulation/fsma/
ucm459719.htm). We have summarized
the relevant comments received and
provided our responses below.
(Comment 1) Many comments
supported the proposed extension of
compliance dates for the agricultural
water provisions for covered produce
other than sprouts. One comment stated
that the extension would allow covered
farms an opportunity to continue a
dialogue with FDA around the best
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approaches to implementing the
agricultural water provisions. An
association said it ‘‘strongly supported’’
the proposed extension, that the
agricultural water provisions are very
complex, and explained it had been
working to educate its members about
the requirements but found that
developing practical advice was a
challenge given the complexity. Another
organization expressed its support for
the proposed extension and stated that
the agricultural water provisions are
complicated and difficult to understand.
Another individual wrote in support of
the extension, contending that covered
farms and other stakeholders have been
confused by the requirements, and
opined that an extension would be
particularly helpful to smaller covered
farms that could use the additional time
to understand and implement these
provisions.
(Response 1) These comments are
consistent with the feedback we have
been receiving on the complexity of the
agricultural water provisions from
stakeholders since the produce safety
final rule published in 2015. We have
repeatedly heard the message relayed in
these comments—that the requirements
of subpart E, particularly the sampling
and testing provisions, are complicated
to understand, and questions remain
about how to implement them in a
practical manner. Accordingly, we have
decided to finalize the extension as
proposed.
(Comment 2) Some comments
opposed FDA’s proposal to extend the
compliance dates because they did not
believe we had sufficiently justified the
proposed delay, or its length. These
comments noted that the compliance
dates for certain agricultural water
testing requirements were already later
than the compliance dates for the rest of
the produce safety regulation. These
comments also stated that FDA had
already sufficiently addressed
stakeholder concerns through the
rulemaking process, noting that we
revised the agricultural water
requirements as a result of comments on
the proposed and supplemental rules.
Some comments also encouraged the
Agency to withdraw the proposed rule
and focus on implementing the produce
safety regulation on time; these
comments also noted the public health
benefits of the produce safety
regulation.
(Response 2) While we share the goal
of public health expressed in these
comments, we believe that a delay is
necessary and justified for reasons
different than those set out in the final
rule for the changes to the agricultural
water requirements. The feedback we
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have received since the final rule was
published about the complexity and the
attendant challenges with the produce
safety regulation’s agricultural water
requirements has been frequent and
consistent and has come from growers
of many commodities in many regions.
This feedback is new and is in addition
to the comments on the proposed rule.
Since the final rule was published,
many covered farms, both individually
and in groups via associations, have
strenuously expressed concerns,
particularly around the complexity of
the sampling and testing provisions. On
numerous farm visits and industry
gatherings across the country,
stakeholders have frequently
communicated to us that they view the
agricultural water regulatory scheme as
too complex and too burdensome, and
have objected that it does not
sufficiently allow for a variety of water
uses and availabilities. In the face of
these widespread and steady concerns,
including new concerns that were not
expressed in response to the proposed
rule, we proposed this compliance date
extension, for the purpose of further
engaging stakeholders and determining
what can be done to consider and
address the concerns we have heard.
Many comments to this docket repeat
and reinforce what we have been
hearing. We therefore conclude it is in
the public’s interest for us to institute
this delay so that we may further
collaborate with an array of stakeholders
and pursue solutions that will allow us
to achieve the shared goal of improved
produce safety in a way that is more
workable for covered farms.
The length of this delay in
compliance dates was chosen to allow
us sufficient time to explore these
challenges with stakeholders and
experts, and pursue solutions that
improve the workability of these
provisions. Covered farms also need a
significant amount of time to prepare for
compliance after the solutions are
determined. A shorter time period
would not have been sufficient for both
robust stakeholder engagement and for
covered farms to transition to
implementation.
(Comment 3) Some comments
opposed FDA’s proposal to extend the
agricultural water compliance dates, in
general because they concluded the
extension would harm consumers more
than it would help covered farms. Some
of these comments noted that FDA’s
cost-benefit analysis indicates that this
delay would impose a burden on
consumers that outweighs any gains that
may accrue to producers. Some
comments contended that the extension
has the potential to increase the risk of
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illness and death by potentially more
than 730,000 additional cases of
foodborne illness. Some comments
noted that the proposed compliance
date extension would mean covered
farms would not be required to comply
with these provisions until 11–13 years
after FSMA was enacted, thereby
delaying benefits to the public.
(Response 3) FDA remains committed
to ensuring that the produce safety rule
addresses the risks associated with
agricultural water. We note that produce
remains subject to the adulteration
provisions of the FD&C Act during this
extension of the compliance dates, and
the agency encourages farms to focus
their attention on good agricultural
practices to maintain and protect the
quality of their water sources. (See, e.g.,
FDA’s ‘‘Guide to Minimize Microbial
Food Safety Hazards for Fresh Fruits
and Vegetables,’’ at https://
www.fda.gov/Food/Guidance
Regulation/GuidanceDocuments
RegulatoryInformation/
ucm064574.htm). We have, however,
determined that it will serve the public
health best to take time now to engage
stakeholders and discern how best to
achieve public health protections in the
covered produce agricultural water
arena. FDA believes that ignoring the
widespread concerns raised about
complexity and serious questions about
how the requirements can be
implemented in practical ways on farms
is also likely to reduce the estimated
public health benefits of the agricultural
water provision of the rule. Farms that
cannot understand the requirements and
determine how to implement the
requirements are not likely to be
realizing full food safety measures. We
thus believe it is critical to address the
issues we have heard about the
complexity of the final rule and the
diversity of use and source of
agricultural water, and the variety of
factors that impact agricultural water.
The agency also believes that further
collaboration with stakeholders to
understand the source of the complexity
and develop practical solutions is
necessary to best allow us to achieve the
shared goal of improved produce safety
in a way that is more workable for
covered farms.
The economic analysis we conducted
for the produce safety final rule, in
keeping with our standard practice,
evaluated the costs and benefits of the
rule in its first 10 years, or 2016–2025.
We analyzed the costs and benefits of
this extension over the same time
horizon (2016–2025). We estimated that
this extension would translate to a
savings of $12 (10) million for covered
farms (annualized at 3 (7) percent over
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those 10 years), because we estimated
covered farms would delay making
additional investments to initially
comply with the agricultural water
provisions until the arrival of the
extended compliance dates. Because our
economic analysis spans ten years
starting with the produce safety rule
effective date, the delay in those initial
investments shows as a savings over
those 10 years, but over the longer term
may be viewed as costs deferred rather
than saved. Using the same time horizon
(2016–2025), we also estimated that this
extension would reduce expected
benefits from the rule as a whole during
those 10 years from $800 ($740) million
to $696 ($644) million, annualized at 3
percent (7 percent) over those 10 years.
We do not know how the commenter
arrived at the estimate that this
extension could contribute to more than
730,000 additional cases of foodborne
illness. We estimate that approximately
31,300 illnesses would not be prevented
during the specified 10-year time
horizon as a result of this extension.2
Because we have not yet decided how
to address the concerns that have been
raised about the practicality of the
requirements, we cannot estimate the
economic impact or the effect on
foodborne illness rates of any solutions
that we might implement in the future.
With the delay of the compliance
dates, we intend to lay the groundwork
for a successful implementation, which
will benefit all stakeholders. We will
use this time to engage with all
stakeholders and consult with experts to
determine how to implement, explain,
and/or revise the agricultural water
provisions in ways that reduce
complexity and improve their
workability for covered farms while still
attaining for the public the benefits of
science-based agricultural water
standards for covered produce. We will
also use the time to continue our
outreach and educational efforts, so that
the myriad types of covered farms will
have the opportunity to prepare for
successful implementation.
(Comment 4) Some comments
opposed FDA’s proposal to extend
compliance dates because they felt that
the proposed rule was too broad in that
it extends the compliance date for other
2 We arrive at this estimate by taking the decrease
in the annualized benefits between the original
produce safety rule and the rule with this extension
(about $104 million and $96 million at 3 percent
and 7 percent, respectively, over 10 years) and
dividing it by the average cost per foodborne illness
associated with covered produce other than sprouts.
We estimate that approximately 30,103 and 32,554
illnesses annualized at 3 percent and 7 percent,
respectively, that we estimate would not be
prevented during the specified 10-year time
horizon.
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agricultural water provisions in subpart
E that are not dependent on an analysis
of multiyear water profile (e.g.,
requirement for growers to inspect and
repair water distribution infrastructure,
monitor for the buildup of organic
material in wash tanks and coolers,
maintain and monitor the temperature
of water to minimize microbiological
risk, and keeping records of the
scientific support for food safety
interventions). Comments argued that
some subpart E requirements are not
complex, and it would not be difficult
for covered farms to comply with such
requirements by the original compliance
dates. Comments also noted some thirdparty audits require compliance with
standards that are similar to parts of
subpart E, implying that some covered
farms are already complying with
similar provisions for that purpose.
(Response 4) FDA considered
proposing to extend just the provisions
in subpart E that, under the produce
safety final rule, had a compliance date
2 years later than the rest of subpart E
(see table 2), but we determined that
there were other provisions in subpart E
that were equally complex and
challenging for stakeholders,
particularly other sampling and testing
provisions (see, e.g., § 112.46(b)(1)
(testing requirement originally subject to
the ‘‘earlier’’ compliance date in the
context of untreated surface water)).
Accordingly, retaining the original
bifurcated structure was not an option.
We have heard repeatedly from
stakeholders that the compliance date
structure under subpart E is confusing,
so extending compliance dates for both
a subset of the originally-not-extended
provisions of subpart E, together with
the originally-extended provisions of
subpart E, would mean adding another
layer of confusion to the subpart E
compliance date situation, and that did
not seem wise or workable.
Some third-party audits include
agricultural water requirements with
which farms must comply to obtain a
passing audit or certification, and some
of those requirements may be similar to
provisions in subpart E. Although some
segments of the industry do undergo
third-party audits, that fact did not
dissuade us from the conclusion that
there is a need to extend the compliance
date for all of subpart E (for covered
produce other than sprouts), which is
based on significant feedback received
from stakeholders since publication of
subpart E in the produce safety final
rule as well as comments on the
extension proposed rule.
(Comment 5) Some comments argued
that FDA failed to explain the nature of
the confusion over the rule’s
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Fmt 4700
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9711
compliance date structure that caused
us to propose a simplification to that
structure.
(Response 5) As evidenced by other
comments, there was confusion over the
compliance dates in subpart E and some
stakeholders found it challenging to
discern exactly which regulatory
requirements were subject to the longer
compliance period. One comment noted
that simply determining the relevant
compliance date is a challenge and said
simplifying the compliance date
structure would help. Other comments
noted being confused by the existing
compliance date structure. We conclude
there is sufficient justification for us to
simplify the subpart E compliance date
structure.
(Comment 6) Even with the
compliance date extension and
simplification we proposed in
September 2017 and are finalizing here,
some comments expressed confusion
about the meaning of the compliance
date with respect to initiating sampling
versus completing the microbial water
quality profile (MWQP). One comment
specifically requested that the new
compliance dates mean the dates on
which farms must start to conduct the
initial survey to develop the MWQP.
(Response 6) Farms are not required
to have completed a MWQP by their
compliance date. A farm’s compliance
date means the date on which the farm
must begin sampling a water source for
its initial survey, which will eventually
result in a MWQP.
We note that this issue was addressed
in the 2016 final rule that extended and
clarified compliance dates for certain
FSMA provisions (81 FR 57784 at
57793–94). However, we recognize that
there is still confusion about when the
MWQP must be completed under the
simplified compliance date structure we
are finalizing here. We are therefore
clarifying that farms are not required to
have already developed a completed
MWQP as of their new compliance date.
Rather, farms must begin sampling and
testing their untreated water sources in
accordance with § 112.46(b)(1), as
applicable, by their compliance date. If
the compliance date is not an
appropriate time to engage in the
relevant sampling and testing
activities—for example, because of the
requirement in § 112.46(b)(1)(ii) that
samples be representative of your use of
the water—then compliance must begin
by the first relevant time period that
occurs after the compliance date.
To elaborate on what this would mean
in practical terms, for a farm that is not
small or very small, compliance must
begin by the first relevant time period
that occurs on or after January 26, 2022.
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For example, if a farm that is not small
or very small only uses an untreated
water source for agricultural water in
May, a compliance date of January 26,
2022, would indicate that sample
collection under § 112.46(b)(1) must
take place in May 2022, as that is the
time in which water samples collected
would be representative of their use of
the water. Farms that wish to develop or
begin developing their MWQP prior to
their compliance date are welcome to do
so; but in the above example, FDA
would not expect sample collection to
have begun prior to May 2022.
To provide a few examples related to
the number and timing of samples, all
of the following possible approaches are
acceptable for farms that are not small
or very small:
• Beginning in 2022, conducting an
initial survey of an untreated surface
water source by taking 10 samples per
year over 2 years (10 in 2022 and 10 in
2023) for a total of 20 samples in
accordance with § 112.46(b)(1)(i)(A);
calculating the MWQP for the first time
upon completing the 20-sample data set
in 2023; and applying any necessary
corrective actions under § 112.45(b) as
soon as practicable and no later than the
following year (e.g., during the 2024
growing season).
• Beginning in 2022, conducting an
initial survey of an untreated surface
water source by taking 5 samples per
year over 4 years (5 in 2022, 5 in 2023,
5 in 2024, and 5 in 2025) for a total of
20 samples, in accordance with
§ 112.46(b)(1)(i)(A); calculating the
MWQP for the first time upon
completing the 20-sample data set in
2025; and applying any necessary
corrective actions under § 112.45(b) as
soon as practicable and no later than the
following year (e.g., during the 2026
growing season).
• Beginning in 2022, conducting an
initial survey of an untreated ground
water source by taking 4 samples during
the 2022 growing season in accordance
with § 112.46(b)(1)(i)(B); calculating the
MWQP for the first time upon
completing the 4-sample data set at the
end of the 2022 growing season; and
applying any necessary corrective
actions under § 112.45(b) as soon as
practicable and no later than the
following year (e.g., during the 2023
growing season).
(Comment 7) Some comments
requested additional outreach and
education as FDA explores
modifications to the agricultural water
testing provisions.
(Response 7) FDA intends to continue
to work with an array of stakeholders to
explore and address the concerns
around subpart E. As described above,
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15:57 Mar 15, 2019
Jkt 247001
we will be implementing a rigorous
stakeholder engagement plan over the
course of several months. If we
determine that changes to subpart E are
necessary, that would require notice and
comment rulemaking and thus the
public would have an opportunity to
comment on any proposed changes. If
we determine that we can address
concerns through guidance, such a
guidance would be considered ‘‘Level
1’’ and would be subject to the notice
and comment procedures outlined in
§ 10.115(g), which is part of FDA’s Good
Guidance Practices regulations. We also
remain committed to working with
covered farms to prepare for
compliance, through outreach, training
and education, and other collaboration.
(Comment 8) Some comments stated
the proposed extension is contrary to
Congress’ intent and the plain language
of FSMA, noting that the statute
included a deadline for the produce
safety final rule.
(Response 8) We do not agree that
delaying the compliance date for
subpart E is contrary to Congress’s
intent or the plain language of the
statute. FSMA required FDA to establish
science- and risk-based minimum
standards for the safe production and
harvesting of produce for human
consumption (see section 419(a)(1)(A) of
the FD&C Act (21 U.S.C. 350h(a)(1)(A))),
which we have done by promulgating
the produce safety regulation. Extending
the compliance dates for subpart E (for
covered produce other than sprouts)
will allow us to evaluate how we can
either improve the requirements or
implement them in a way that is less
confusing and more workable for
covered farms, in light of the feedback
we have received about subpart E, while
still protecting the public health.
Although FSMA includes deadlines
for issuing the proposed and final rules,
there is nothing in the language or spirit
of the statute that is contrary to FDA
doing its due diligence to examine how
we can achieve the public health
regulatory objectives contained in the
rule in a way that is more practical for
covered farms. We reiterate that we are
not changing the compliance dates for
the entire produce safety regulation, just
subpart E for covered produce other
than sprouts.
(Comment 9) Comments stated that
FDA should clearly communicate its
expectations of agricultural water users
during the extension.
(Response 9) With this final rule, we
are extending the compliance dates for
subpart E of the produce safety
regulation for covered produce other
than sprouts. FDA will therefore not
expect growers of covered produce
PO 00000
Frm 00020
Fmt 4700
Sfmt 4700
(other than sprouts) to implement
subpart E until the new compliance
dates. In the meantime, farms should
focus their attention on good
agricultural practices to maintain and
protect the quality of their water
sources. (See, e.g., FDA’s ‘‘Guide to
Minimize Microbial Food Safety
Hazards for Fresh Fruits and
Vegetables,’’ at https://www.fda.gov/
Food/GuidanceRegulation/
GuidanceDocuments
RegulatoryInformation/
ucm064574.htm). Farms currently
testing their water may choose to
continue with their current water testing
programs, and farms that are not
currently testing their water may choose
to begin doing so.
IV. Economic Analysis of Impacts
We have examined the impacts of this
rule under Executive Order 12866,
Executive Order 13563, Executive Order
13771, the Regulatory Flexibility Act (5
U.S.C. 601612), and the Unfunded
Mandates Reform Act of 1995 (Pub. L.
104–4). Executive Orders 12866 and
13563 direct us to assess all costs and
benefits of available regulatory
alternatives and, when regulation is
necessary, to select regulatory
approaches that maximize net benefits
(including potential economic,
environmental, public health and safety,
and other advantages; distributive
impacts; and equity). Executive Order
13771 requires that the costs associated
with significant new regulations ‘‘shall,
to the extent permitted by law, be offset
by the elimination of existing costs
associated with at least two prior
regulations.’’ We believe that this final
rule is an economically significant
regulatory action as defined by
Executive Order 12866.
The Regulatory Flexibility Act
requires Agencies to analyze regulatory
options that will minimize any
significant impact of a rule on small
entities. Because this final rule only
extends the compliance dates for certain
provisions of the produce safety
regulation, we certify that this final rule
will not have a significant economic
impact on a substantial number of small
entities.
The Unfunded Mandates Reform Act
of 1995 (section 202(a)) requires us to
prepare a written statement, which
includes an assessment of anticipated
costs and benefits, before proposing
‘‘any rule that includes any Federal
mandate that may result in the
expenditure by state, local, and tribal
governments, in the aggregate, or by the
private sector, of $100,000,000 or more
(adjusted annually for inflation) in any
one year.’’ The current threshold after
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adjustment for inflation is $150 million,
using the most current (2017) Implicit
Price Deflator for the Gross Domestic
Product. This final rule will not result
in an expenditure in any year that meets
or exceeds this amount.
This rule extends, for non-sprout
covered produce, the compliance date
for all of the provisions of subpart E to
4 years after the relevant farm’s
compliance date for all other provisions
of the produce safety regulation (which
varies based on establishment size). The
estimated costs and benefits accrued in
any given year of compliance with the
produce safety regulation, relative to the
first year of compliance, do not change.
However, because the compliance dates
for certain provisions are extended, the
discounted value of both total costs and
total benefits decrease.
In the final regulatory impact analysis
of subpart E of the produce safety
regulation, we only considered
§§ 112.42, 112.44, 112.45(a)(2),
112.45(b)(3), 112.46(b), and 112.46(c) to
result in a cost. Therefore, while subpart
E has other provisions, only the
aforementioned provisions are relevant
to and addressed in this cost and benefit
analysis.
There is a reduction in costs (i.e., cost
savings) associated with extending, for
non-sprout covered produce, the
compliance date for all of the provisions
of subpart E to 4 years after the relevant
farm’s compliance date for the rest of
the produce safety regulation. With
respect to their non-sprout covered
produce, covered farms have 4 years
from the compliance date for the other
provisions of produce safety regulation
to comply with the provisions in
subpart E. Thus, while all initial startup
costs and recurring costs remain the
same as estimated in the final regulatory
impact analysis for the produce safety
regulation (Ref. 1), the annualized total
costs, discounted at 3 (7) percent over
10 years, decrease from $291 ($265)
million to $280 ($254) million, resulting
in a savings of $12 ($10) million.3 The
present value of total costs, discounted
at 3 (7) percent over 10 years, decreases
from about $2.5 ($1.9) billion to about
$2.4 ($1.8) billion, resulting in a savings
9713
of about $99 ($74) million. No
additional costs would be incurred by
state, local, and tribal governments or
the private sector as a result of this rule.
There is a reduction in benefits
associated with extending the
compliance dates as described
previously. Consumers eating nonsprout covered produce will not enjoy
the potential health benefits (i.e.,
reduced risk of illness) provided by the
provisions of subpart E until 2 to 4 years
(depending on the specific provision)
later than originally established in the
produce safety regulation. Thus, the
annualized total benefits to consumers,
discounted at 3 (7) percent over 10
years, decrease by $104 ($96) million
from $800 ($740) million to $696 ($644)
million. The present value of total
benefits, discounted at 3 (7) percent
over 10 years, decreases from about $6.8
($5.2) billion to about $5.9 ($4.5) billion.
Estimated changes in benefits and costs
as a result of this extension are
summarized in the following table.
TABLE 5—SUMMARY OF CHANGES TO BENEFITS AND COSTS AS A RESULT OF THE FINAL RULE
Units
Primary
estimate
Category
Forgone Benefits:
Annualized ................................................................................................
Monetized $millions/year ..........................................................................
Forgone Costs:
Annualized ................................................................................................
Monetized $millions/year ..........................................................................
In line with Executive Order 13771, in
table 6 we estimate present and
annualized values of costs and cost
Year dollars
Discount rate
(%)
Period
covered
$96
104
2017
2017
7
3
2016–2025
2016–2025
10
12
2017
2017
7
3
2016–2025
2016–2025
savings over an infinite time horizon.
Based on these cost-savings, this final
rule will be considered a deregulatory
action under Executive Order 13771.
TABLE 6—EXECUTIVE ORDER 13771 SUMMARY TABLE (IN $ MILLIONS 2016 DOLLARS, OVER AN INFINITE TIME HORIZON)
Primary
estimate
(7%)
Item
Present Value of Cost Savings ...............................................................................................................................
Annualized Cost Savings .........................................................................................................................................
$72
5
Primary
estimate
(3%)
$97
3
We have developed a comprehensive
Economic Analysis of Impacts that
assesses the impacts of the final rule.
The full analysis of economic impacts is
available in the docket for this rule (Ref.
2) at https://www.regulations.gov, and at
https://www.fda.gov/AboutFDA/Reports
ManualsForms/Reports/Economic
Analyses/default.htm.
V. Analysis of Environmental Impact
VI. Paperwork Reduction Act of 1995
We have determined under 21 CFR
25.30(j) that this action is of a type that
does not individually or cumulatively
have a significant effect on the human
environment. Therefore, neither an
environmental assessment nor an
environmental impact statement is
required.
This rule contains no collection of
information. Therefore, clearance by the
Office of Management and Budget under
the Paperwork Reduction Act of 1995 is
not required.
3 The $12 million and $10 million figures are
rounded. The costs decrease from $291.5 ($264.8)
million to $279.8 ($254.3) million, resulting in a
savings of $11.6 ($10.5) million.
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Federal Register / Vol. 84, No. 52 / Monday, March 18, 2019 / Rules and Regulations
VII. Federalism
We have analyzed this rule in
accordance with the principles set forth
in Executive Order 13132. FDA has
determined that the rule does not
contain policies that have substantial
direct effects on the States, on the
relationship between the National
Government and the States, or on the
distribution of power and
responsibilities among the various
levels of government. Accordingly, we
conclude that the rule does not contain
policies that have federalism
implications as defined in the Executive
order and, consequently, a federalism
summary impact statement is not
required.
VIII. Consultation and Coordination
With Indian Tribal Governments
IX. References
The following references are on
display in the Dockets Management
Staff (HFA–305), Food and Drug
Administration, 5630 Fishers Lane, Rm.
1061, Rockville, MD 20852 and are
available for viewing by interested
persons between 9 a.m. and 4 p.m.,
Monday through Friday; they are also
available electronically at https://
www.regulations.gov. FDA has verified
the website addresses, as of the date this
document publishes in the Federal
Register, but websites are subject to
change over time.
1. FDA, ‘‘Final Regulatory Impact
Analysis, Standards for the Growing,
Harvesting, Packing and Holding of
Produce for Human Consumption.’’
November 2015. Available at: https://
www.fda.gov/AboutFDA/Reports
ManualsForms/Reports/Economic
Analyses/ucm472310.htm.
2. FDA, ‘‘Final Regulatory Impact
Analysis, Final Regulatory Flexibility
Analysis, and Unfunded Mandates
Reform Act Analysis for the Standards
for the Growing, Harvesting, Packing,
and Holding of Produce for Human
15:57 Mar 15, 2019
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[FR Doc. 2019–04652 Filed 3–15–19; 8:45 am]
BILLING CODE 4164–01–P
DEPARTMENT OF HOMELAND
SECURITY
33 CFR Part 165
RIN 1625–AA87
Security Zones; Corpus Christi Ship
Channel, Corpus Christi, TX
Coast Guard, DHS.
Temporary final rule.
AGENCY:
SUMMARY: The Coast Guard establishes
two security zones. One of the zones is
a temporary fixed security zone for the
receiving facility’s mooring basin while
the Liquefied Natural Gas Carrier
(LNGC) MARVEL FALCON is moored at
the facility. The other zone is a moving
security zone encompassing all
navigable waters within a 500-yard
radius around the LNGC MARVEL
FALCON while the vessel transits with
cargo in the La Quinta Channel and
Corpus Christi Ship Channel in Corpus
Christi, TX. The security zones are
needed to protect personnel, vessels,
and the marine environment from
potential hazards created by Liquified
Natural Gas (LNG) cargo aboard the
vessel. Entry of vessels and persons into
these zones is prohibited unless
specifically authorized by the Captain of
the Port Sector Corpus Christi.
DATES: This rule is effective without
actual notice from 12 a.m. through 11:59
p.m. on March 18, 2019. For the
purposes of enforcement, actual notice
will be used from March 11, 2019 until
March 18, 2019.
ADDRESSES: To view documents
mentioned in this preamble as being
available in the docket, go to https://
www.regulations.gov, type USCG–2019–
0156 in the ‘‘SEARCH’’ box and click
‘‘SEARCH.’’ Click on Open Docket
Folder on the line associated with this
rule.
FOR FURTHER INFORMATION CONTACT: If
you have questions on this rule, call or
email Petty Officer Kevin Kyles, Sector
Corpus Christi Waterways Management
PO 00000
Frm 00022
SUPPLEMENTARY INFORMATION:
CFR Code of Federal Regulations
COTP Captain of the Port Sector Corpus
Christi
DHS Department of Homeland Security
FR Federal Register
LNGC Liquefied Natural Gas Carrier
NPRM Notice of proposed rulemaking
§ Section
U.S.C. United States Code
II. Background Information and
Regulatory History
Coast Guard
ACTION:
Division, U.S. Coast Guard; telephone
361–939–5125, email Kevin.L.Kyles@
uscg.mil.
I. Table of Abbreviations
Dated: March 6, 2019.
Scott Gottlieb,
Commissioner of Food and Drugs.
[Docket Number USCG–2019–0156]
We have analyzed this rule in
accordance with the principles set forth
in Executive Order 13175. We have
determined that the rule does not
contain policies that have substantial
direct effects on one or more Indian
tribes, on the relationship between the
Federal Government and Indian tribes,
or on the distribution of power and
responsibilities between the Federal
Government and Indian tribes.
Accordingly, we conclude that the rule
does not contain policies that have
tribal implications as defined in the
Executive order and, consequently, a
tribal summary impact statement is not
required.
VerDate Sep<11>2014
Consumption; Extension of Compliance
Dates for Subpart E; Final Rule,’’ 2019.
Available at: https://www.fda.gov/About
FDA/ReportsManualsForms/Reports/
EconomicAnalyses/.
Fmt 4700
Sfmt 4700
The Coast Guard is issuing this
temporary rule without prior notice and
opportunity to comment pursuant to
authority under section 4(a) of the
Administrative Procedure Act (APA) (5
U.S.C. 553(b)). This provision
authorizes an agency to issue a rule
without prior notice and opportunity to
comment when the agency for good
cause finds that those procedures are
‘‘impracticable, unnecessary, or contrary
to the public interest.’’ Under 5 U.S.C.
553(b)(3)(B), the Coast Guard finds that
good cause exists for not publishing an
NPRM with respect to this rule because
it is impracticable. We must establish
these security zones by March 11, 2019
and lack sufficient time to provide a
reasonable comment period and then
consider those comments before issuing
the rule.
Under 5 U.S.C. 553(d)(3), the Coast
Guard finds that good cause exists for
making this rule effective less than 30
days after publication in the Federal
Register. Delaying the effective date of
this rule would be contrary to the public
interest because immediate action is
needed to provide for the security of the
vessel.
III. Legal Authority and Need for Rule
The Coast Guard is issuing this rule
under authority in 46 U.S.C. 70034. The
COTP has determined that potential
hazards associated with LNGC MARVEL
FALCON between March 11, 2019 and
March 18, 2019 will be a security
concern while the vessel is moored at
the receiving facility and within a 500yard radius of the vessel while the
vessel transits with cargo.
IV. Discussion of the Rule
This rule establishes two security
zones around LNGC MARVEL FALCON
from March 11, 2019 through March 18,
2019. A fixed security zone will be in
effect in the mooring basin bound by
27°52′53.38″ N, 097°16′20.66″ W on the
northern shoreline; thence to
E:\FR\FM\18MRR1.SGM
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Agencies
[Federal Register Volume 84, Number 52 (Monday, March 18, 2019)]
[Rules and Regulations]
[Pages 9706-9714]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2019-04652]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
21 CFR Part 112
[Docket No. FDA-2011-N-0921]
RIN 0910-AH93
Standards for the Growing, Harvesting, Packing, and Holding of
Produce for Human Consumption; Extension of Compliance Dates for
Subpart E
AGENCY: Food and Drug Administration, HHS.
ACTION: Final rule.
-----------------------------------------------------------------------
SUMMARY: The Food and Drug Administration (FDA, the Agency, or we) is
extending, for covered produce other than sprouts, the dates for
compliance with the agricultural water provisions in the ``Standards
for the Growing, Harvesting, Packing, and Holding of Produce for Human
Consumption'' rule. We are extending the compliance dates to address
questions about the practical implementation of compliance with certain
provisions and to consider how we might further reduce the regulatory
burden or increase flexibility while continuing to protect public
health.
DATES: As of March 18, 2019 the compliance dates for the agricultural
water provisions (subpart E) in the Standards for the ``Growing,
Harvesting, Packing, and Holding of Produce for Human Consumption''
rule (November 27, 2015, 80 FR 74354), for covered produce other than
sprouts, are delayed to January 26, 2024, for very small businesses,
January 26, 2023, for small businesses, and January 26, 2022, for all
other businesses.
FOR FURTHER INFORMATION CONTACT: Samir Assar, Center for Food Safety
and Applied Nutrition (HFS-317), Food and Drug Administration, 5001
Campus Dr., College Park, MD 20740, 240-402-1636.
SUPPLEMENTARY INFORMATION:
Table of Contents
I. Executive Summary
II. Background
III. Analysis and Response to Public Comments
IV. Economic Analysis of Impacts
V. Analysis of Environmental Impact
VI. Paperwork Reduction Act of 1995
VII. Federalism
VIII. Consultation and Coordination With Indian Tribal Governments
IX. References
I. Executive Summary
The final rule extends, for covered produce other than sprouts, the
dates for compliance with the agricultural water provisions in the
``Standards for the Growing, Harvesting, Packing, and Holding of
Produce for Human Consumption'' rule. The agricultural water provisions
are contained in subpart E of that rule. We are also simplifying the
compliance date structure under subpart E as applied to non-sprout
covered produce, while retaining date-staggering based on size. The new
compliance dates for the agricultural water requirements in subpart E
for non-sprout covered produce are January 26, 2024, for very small
businesses; January 26, 2023, for small businesses; and January 26,
2022, for all other businesses.
The final rule does not alter the requirements in subpart E and
therefore the estimated costs and benefits accrued in any given year of
compliance with the produce safety regulation, relative to the first
year of compliance, do not change. However, because the compliance
dates for the agricultural water provisions are extended, the
discounted value of both total costs and total benefits decrease.
The impact of this final rule is summarized in the following table.
Table 1--Summary of Changes to Benefits and Costs as a Result of the Final Rule
----------------------------------------------------------------------------------------------------------------
Units
Primary -----------------------------------------------
Category estimate Discount rate
Year dollars (%) Period covered
----------------------------------------------------------------------------------------------------------------
Forgone Benefits:
[[Page 9707]]
Annualized.................................. $96 2017 7 2016-2025
Monetized $millions/year.................... 104 2017 3 2016-2025
Forgone Costs:
Annualized.................................. 10 2017 7 2016-2025
Monetized $millions/year.................... 12 2017 3 2016-2025
----------------------------------------------------------------------------------------------------------------
II. Background
This extension of compliance dates concerns one of the seven
foundational rules that we have established in Title 21 of the Code of
Federal Regulations (21 CFR), Part 112 as part of our implementation of
the FDA Food Safety Modernization Act (FSMA; Pub. L. 111-353):
``Standards for the Growing, Harvesting, Packing, and Holding of
Produce for Human Consumption'' (the produce safety regulation,
published in the Federal Register of November 27, 2015, 80 FR 74354)
(https://www.fda.gov/fsma). We proposed this extension in a proposed
rule published on September 13, 2017 (82 FR 42963). We have reviewed
the comments submitted in response to the proposed rule, and we respond
to those comments in section II. In this final rule we are extending
the compliance dates as proposed.
In the preamble of the final rule establishing the produce safety
regulation, we stated that the produce safety regulation would be
effective on January 26, 2016, and provided for compliance dates of 1
to 6 years from the effective date depending on farm size, commodity,
and provision(s) (see table entitled ``compliance dates'' in the
preamble of the final rule establishing the produce safety regulation,
80 FR 74354 at 74357, as corrected in a technical amendment at 81 FR
26466, May 3, 2016). (Some of the compliance dates identified in the
technical amendment fall on weekends (i.e., January 26, 2019, is a
Saturday and January 26, 2020, is a Sunday) and should therefore be
read as referring to the next business day (i.e., January 28, 2019, and
January 27, 2020, respectively). We use the latter dates throughout
this document.)
For the majority of agricultural water provisions at subpart E (and
for most of the other provisions in the rule), with respect to covered
produce other than sprouts, we provided compliance periods of 4 years
from the effective date of the rule for very small businesses, 3 years
for small businesses, and 2 years for all other businesses.\1\ We
provided an additional 2 years beyond those compliance periods for
certain water quality requirements in Sec. 112.44 and related
provisions in Sec. Sec. 112.45 and 112.46. See table 2.
---------------------------------------------------------------------------
\1\ Under the produce safety regulation, a farm is a very small
business if, on a rolling basis, the average annual monetary value
of produce it sold during the previous 3-year period is no more than
$250,000. A farm is a small business if, on a rolling basis, the
average annual monetary value of produce it sold during the previous
3-year period is no more than $500,000; and the farm is not a very
small business. See 21 CFR 112.3.
---------------------------------------------------------------------------
In a final rule, ``The Food and Drug Administration Food Safety
Modernization Act; Extension and Clarification of Compliance Dates for
Certain Provisions of Four Implementing Rules'' (81 FR 57784, August
24, 2016) we also extended the compliance date for certain ``customer
provisions'' in four of the seven foundational rules that we have
established as part of our implementation of FSMA, including the
produce safety regulation (Sec. 112.2(b)(3)). In that final rule, we
also clarified how we interpret the compliance dates for certain
agricultural water testing provisions established in the produce safety
regulation.
Table 2--As Stated in Produce Safety Regulation, Compliance Dates for
Requirements in Subpart E (Agricultural Water) for Covered Activities
Involving Covered Produce (Except Sprouts Subject to Subpart M)
------------------------------------------------------------------------
Extended compliance date of
Compliance dates of 2-4 years additional 2 years beyond the
applicable to the farm based on its compliance date based on size of
size farm
------------------------------------------------------------------------
Sec. 112.41. Sec. 112.44.
Sec. 112.42. Sec. 112.45(a) with respect to
Sec. 112.44(a) criterion.
Sec. 112.43.
Sec. 112.45(b).
Sec. 112.45(a) with respect to Sec. 112.46(b)(1) with respect to
safe and adequate standard. untreated ground water.
Sec. 112.46(a). Sec. 112.46(b)(2) and (b)(3).
Sec. 112.46(b)(1) with respect to Sec. 112.46(c).
untreated surface water.
Sec. 112.47.
Sec. 112.48.
Sec. 112.49.
Sec. 112.50.
------------------------------------------------------------------------
FDA has received feedback from numerous stakeholders raising issues
regarding the practicality of some of the agricultural water
requirements in the produce safety regulation as applied to covered
produce other than sprouts. Many of these concerns relate to the
testing requirements for pre-harvest agricultural water, which are
different for sprouts than they are for other types of covered produce.
We are extending these compliance dates in light of the feedback we
have received. Additional time allows us to consider how to approach
these issues.
[[Page 9708]]
As part of this extension, we are simplifying the subpart E
compliance period structure such that all the compliance dates for
subpart E provisions as applied to non-sprout covered produce will
occur at the same time, retaining date-staggering based on farm size.
Accordingly, covered farms will have 2 years beyond the previously
published compliance dates for the water quality requirements in Sec.
112.44 and related provisions in Sec. Sec. 112.45 and 112.46, to
comply with all of subpart E. Put another way, we are extending the
compliance dates for provisions in the first column of table 2 by 4
years and extending the compliance dates for provisions in the second
column of table 2 by 2 years, so that the compliance dates for non-
sprout covered produce for all provisions of subpart E are those listed
in table 3.
Table 3--Compliance Dates for Requirements in Subpart E for Covered Activities Involving Covered Produce (Except
Sprouts Subject to Subpart M)
----------------------------------------------------------------------------------------------------------------
Time periods starting from the effective date of the November 27, 2015,
produce safety final rule (January 26, 2016)
Size of covered farm -------------------------------------------------------------------------
Compliance period Compliance date
----------------------------------------------------------------------------------------------------------------
Very Small Business................... 8 years............................ January 26, 2024.
Small Business........................ 7 years............................ January 26, 2023.
All Other Businesses.................. 6 years............................ January 26, 2022.
----------------------------------------------------------------------------------------------------------------
This rule is limited in scope to extending the compliance dates for
covered produce other than sprouts. The rule does not address the
underlying requirements in subpart E, but only the compliance dates for
those requirements (for covered produce other than sprouts).
We conducted a qualitative assessment of risk of hazards associated
with produce production during the produce safety rulemaking, which
indicates that agricultural water is a potential route of contamination
of produce during growing, harvesting, and on-farm postharvest
activities and that use of poor agricultural practices could lead to
contamination and illness even where the potential for contamination is
relatively low. We remain firmly committed to science-based minimum
standards directed to agricultural water to minimize the risk of
serious adverse health consequences or death from the use of, or
exposure to, covered produce, including those reasonably necessary to
prevent the introduction of known or reasonably foreseeable hazards
into covered produce, and to provide reasonable assurances that the
produce is not adulterated under section 402 of the Federal Food, Drug,
and Cosmetic Act (FD&C Act) (21 U.S.C. 342). To that end, we have been
pursuing and will continue to pursue a rigorous stakeholder engagement
plan in the coming months as we consider the practical implementation
of the agricultural water requirements and how to best achieve these
important public health objectives. Along with farmers and others in
the produce industry, in February 2018 we participated in a summit at
which participants proposed and discussed potential approaches to
addressing concerns with the existing agricultural water requirements.
We are also continuing visits to farms throughout the country to
further refine our understanding of the myriad variations in
agricultural water sources and uses. We will continue to consult with
experts in produce safety, water systems, and water microbiology, from
both the public and private sectors, to take advantage of the very
latest scientific developments and conclusions, particularly around
water quality criteria, sampling, and testing.
This rule does not change the compliance dates for sprouts. In the
final produce safety regulation, we provided staggered compliance
periods based on farm size for covered activities involving sprouts.
The compliance date for activities involving sprouts for very small
businesses is January 28, 2019. The compliance date for activities
involving sprouts for small businesses is January 26, 2018. The
compliance date for activities involving sprouts for all other
businesses is January 26, 2017. The final produce safety regulation
established sprout-specific requirements on multiple topics, including
agricultural water. The agricultural water requirements for sprouts are
different from the agricultural water requirements for other produce
commodities (compare Sec. Sec. 112.44(a)(1) and 112.44(b)). We have
not received any significant feedback from sprout farms that subpart E
has posed particular challenges. Accordingly, as proposed, we are not
taking action with regard to compliance dates for activities involving
sprouts.
Table 4 summarizes the compliance dates for the produce safety
regulation based on this final rule. Time periods start from the
effective date of the produce safety rule (January 26, 2016) except as
otherwise specified.
BILLING CODE 4164-01-P
[[Page 9709]]
[GRAPHIC] [TIFF OMITTED] TR18MR19.000
BILLING CODE 4164-01-C
III. Analysis and Response to Public Comments
In response to the proposed rule, we received comments from covered
farms, consumer protection groups, groups representing these
stakeholders, and state governments. Many of the comments were
supportive of the proposed extension and simplification of compliance
dates. In this final rule, we respond to comments related to whether
FDA should extend the compliance dates and simplify the compliance date
structure for the agricultural water requirements for covered produce
other than sprouts. We did not consider and do not address comments
that raised issues beyond the narrow scope of the proposed rule,
including comments related to withdrawal or modifications to subpart E
or comments related to broader policy issues. FDA will take these
additional comments into consideration as we consider approaches to
address agricultural water requirements. In this final rule we also do
not address specific questions on the produce safety regulation, but
the Technical Assistance Network remains an available resource for such
questions (https://www.fda.gov/food/guidanceregulation/fsma/ucm459719.htm). We have summarized the relevant comments received and
provided our responses below.
(Comment 1) Many comments supported the proposed extension of
compliance dates for the agricultural water provisions for covered
produce other than sprouts. One comment stated that the extension would
allow covered farms an opportunity to continue a dialogue with FDA
around the best
[[Page 9710]]
approaches to implementing the agricultural water provisions. An
association said it ``strongly supported'' the proposed extension, that
the agricultural water provisions are very complex, and explained it
had been working to educate its members about the requirements but
found that developing practical advice was a challenge given the
complexity. Another organization expressed its support for the proposed
extension and stated that the agricultural water provisions are
complicated and difficult to understand. Another individual wrote in
support of the extension, contending that covered farms and other
stakeholders have been confused by the requirements, and opined that an
extension would be particularly helpful to smaller covered farms that
could use the additional time to understand and implement these
provisions.
(Response 1) These comments are consistent with the feedback we
have been receiving on the complexity of the agricultural water
provisions from stakeholders since the produce safety final rule
published in 2015. We have repeatedly heard the message relayed in
these comments--that the requirements of subpart E, particularly the
sampling and testing provisions, are complicated to understand, and
questions remain about how to implement them in a practical manner.
Accordingly, we have decided to finalize the extension as proposed.
(Comment 2) Some comments opposed FDA's proposal to extend the
compliance dates because they did not believe we had sufficiently
justified the proposed delay, or its length. These comments noted that
the compliance dates for certain agricultural water testing
requirements were already later than the compliance dates for the rest
of the produce safety regulation. These comments also stated that FDA
had already sufficiently addressed stakeholder concerns through the
rulemaking process, noting that we revised the agricultural water
requirements as a result of comments on the proposed and supplemental
rules. Some comments also encouraged the Agency to withdraw the
proposed rule and focus on implementing the produce safety regulation
on time; these comments also noted the public health benefits of the
produce safety regulation.
(Response 2) While we share the goal of public health expressed in
these comments, we believe that a delay is necessary and justified for
reasons different than those set out in the final rule for the changes
to the agricultural water requirements. The feedback we have received
since the final rule was published about the complexity and the
attendant challenges with the produce safety regulation's agricultural
water requirements has been frequent and consistent and has come from
growers of many commodities in many regions. This feedback is new and
is in addition to the comments on the proposed rule. Since the final
rule was published, many covered farms, both individually and in groups
via associations, have strenuously expressed concerns, particularly
around the complexity of the sampling and testing provisions. On
numerous farm visits and industry gatherings across the country,
stakeholders have frequently communicated to us that they view the
agricultural water regulatory scheme as too complex and too burdensome,
and have objected that it does not sufficiently allow for a variety of
water uses and availabilities. In the face of these widespread and
steady concerns, including new concerns that were not expressed in
response to the proposed rule, we proposed this compliance date
extension, for the purpose of further engaging stakeholders and
determining what can be done to consider and address the concerns we
have heard. Many comments to this docket repeat and reinforce what we
have been hearing. We therefore conclude it is in the public's interest
for us to institute this delay so that we may further collaborate with
an array of stakeholders and pursue solutions that will allow us to
achieve the shared goal of improved produce safety in a way that is
more workable for covered farms.
The length of this delay in compliance dates was chosen to allow us
sufficient time to explore these challenges with stakeholders and
experts, and pursue solutions that improve the workability of these
provisions. Covered farms also need a significant amount of time to
prepare for compliance after the solutions are determined. A shorter
time period would not have been sufficient for both robust stakeholder
engagement and for covered farms to transition to implementation.
(Comment 3) Some comments opposed FDA's proposal to extend the
agricultural water compliance dates, in general because they concluded
the extension would harm consumers more than it would help covered
farms. Some of these comments noted that FDA's cost-benefit analysis
indicates that this delay would impose a burden on consumers that
outweighs any gains that may accrue to producers. Some comments
contended that the extension has the potential to increase the risk of
illness and death by potentially more than 730,000 additional cases of
foodborne illness. Some comments noted that the proposed compliance
date extension would mean covered farms would not be required to comply
with these provisions until 11-13 years after FSMA was enacted, thereby
delaying benefits to the public.
(Response 3) FDA remains committed to ensuring that the produce
safety rule addresses the risks associated with agricultural water. We
note that produce remains subject to the adulteration provisions of the
FD&C Act during this extension of the compliance dates, and the agency
encourages farms to focus their attention on good agricultural
practices to maintain and protect the quality of their water sources.
(See, e.g., FDA's ``Guide to Minimize Microbial Food Safety Hazards for
Fresh Fruits and Vegetables,'' at https://www.fda.gov/Food/GuidanceRegulation/GuidanceDocumentsRegulatoryInformation/ucm064574.htm). We have, however, determined that it will serve the
public health best to take time now to engage stakeholders and discern
how best to achieve public health protections in the covered produce
agricultural water arena. FDA believes that ignoring the widespread
concerns raised about complexity and serious questions about how the
requirements can be implemented in practical ways on farms is also
likely to reduce the estimated public health benefits of the
agricultural water provision of the rule. Farms that cannot understand
the requirements and determine how to implement the requirements are
not likely to be realizing full food safety measures. We thus believe
it is critical to address the issues we have heard about the complexity
of the final rule and the diversity of use and source of agricultural
water, and the variety of factors that impact agricultural water. The
agency also believes that further collaboration with stakeholders to
understand the source of the complexity and develop practical solutions
is necessary to best allow us to achieve the shared goal of improved
produce safety in a way that is more workable for covered farms.
The economic analysis we conducted for the produce safety final
rule, in keeping with our standard practice, evaluated the costs and
benefits of the rule in its first 10 years, or 2016-2025. We analyzed
the costs and benefits of this extension over the same time horizon
(2016-2025). We estimated that this extension would translate to a
savings of $12 (10) million for covered farms (annualized at 3 (7)
percent over
[[Page 9711]]
those 10 years), because we estimated covered farms would delay making
additional investments to initially comply with the agricultural water
provisions until the arrival of the extended compliance dates. Because
our economic analysis spans ten years starting with the produce safety
rule effective date, the delay in those initial investments shows as a
savings over those 10 years, but over the longer term may be viewed as
costs deferred rather than saved. Using the same time horizon (2016-
2025), we also estimated that this extension would reduce expected
benefits from the rule as a whole during those 10 years from $800
($740) million to $696 ($644) million, annualized at 3 percent (7
percent) over those 10 years.
We do not know how the commenter arrived at the estimate that this
extension could contribute to more than 730,000 additional cases of
foodborne illness. We estimate that approximately 31,300 illnesses
would not be prevented during the specified 10-year time horizon as a
result of this extension.\2\ Because we have not yet decided how to
address the concerns that have been raised about the practicality of
the requirements, we cannot estimate the economic impact or the effect
on foodborne illness rates of any solutions that we might implement in
the future.
---------------------------------------------------------------------------
\2\ We arrive at this estimate by taking the decrease in the
annualized benefits between the original produce safety rule and the
rule with this extension (about $104 million and $96 million at 3
percent and 7 percent, respectively, over 10 years) and dividing it
by the average cost per foodborne illness associated with covered
produce other than sprouts. We estimate that approximately 30,103
and 32,554 illnesses annualized at 3 percent and 7 percent,
respectively, that we estimate would not be prevented during the
specified 10-year time horizon.
---------------------------------------------------------------------------
With the delay of the compliance dates, we intend to lay the
groundwork for a successful implementation, which will benefit all
stakeholders. We will use this time to engage with all stakeholders and
consult with experts to determine how to implement, explain, and/or
revise the agricultural water provisions in ways that reduce complexity
and improve their workability for covered farms while still attaining
for the public the benefits of science-based agricultural water
standards for covered produce. We will also use the time to continue
our outreach and educational efforts, so that the myriad types of
covered farms will have the opportunity to prepare for successful
implementation.
(Comment 4) Some comments opposed FDA's proposal to extend
compliance dates because they felt that the proposed rule was too broad
in that it extends the compliance date for other agricultural water
provisions in subpart E that are not dependent on an analysis of
multiyear water profile (e.g., requirement for growers to inspect and
repair water distribution infrastructure, monitor for the buildup of
organic material in wash tanks and coolers, maintain and monitor the
temperature of water to minimize microbiological risk, and keeping
records of the scientific support for food safety interventions).
Comments argued that some subpart E requirements are not complex, and
it would not be difficult for covered farms to comply with such
requirements by the original compliance dates. Comments also noted some
third-party audits require compliance with standards that are similar
to parts of subpart E, implying that some covered farms are already
complying with similar provisions for that purpose.
(Response 4) FDA considered proposing to extend just the provisions
in subpart E that, under the produce safety final rule, had a
compliance date 2 years later than the rest of subpart E (see table 2),
but we determined that there were other provisions in subpart E that
were equally complex and challenging for stakeholders, particularly
other sampling and testing provisions (see, e.g., Sec. 112.46(b)(1)
(testing requirement originally subject to the ``earlier'' compliance
date in the context of untreated surface water)). Accordingly,
retaining the original bifurcated structure was not an option. We have
heard repeatedly from stakeholders that the compliance date structure
under subpart E is confusing, so extending compliance dates for both a
subset of the originally-not-extended provisions of subpart E, together
with the originally-extended provisions of subpart E, would mean adding
another layer of confusion to the subpart E compliance date situation,
and that did not seem wise or workable.
Some third-party audits include agricultural water requirements
with which farms must comply to obtain a passing audit or
certification, and some of those requirements may be similar to
provisions in subpart E. Although some segments of the industry do
undergo third-party audits, that fact did not dissuade us from the
conclusion that there is a need to extend the compliance date for all
of subpart E (for covered produce other than sprouts), which is based
on significant feedback received from stakeholders since publication of
subpart E in the produce safety final rule as well as comments on the
extension proposed rule.
(Comment 5) Some comments argued that FDA failed to explain the
nature of the confusion over the rule's compliance date structure that
caused us to propose a simplification to that structure.
(Response 5) As evidenced by other comments, there was confusion
over the compliance dates in subpart E and some stakeholders found it
challenging to discern exactly which regulatory requirements were
subject to the longer compliance period. One comment noted that simply
determining the relevant compliance date is a challenge and said
simplifying the compliance date structure would help. Other comments
noted being confused by the existing compliance date structure. We
conclude there is sufficient justification for us to simplify the
subpart E compliance date structure.
(Comment 6) Even with the compliance date extension and
simplification we proposed in September 2017 and are finalizing here,
some comments expressed confusion about the meaning of the compliance
date with respect to initiating sampling versus completing the
microbial water quality profile (MWQP). One comment specifically
requested that the new compliance dates mean the dates on which farms
must start to conduct the initial survey to develop the MWQP.
(Response 6) Farms are not required to have completed a MWQP by
their compliance date. A farm's compliance date means the date on which
the farm must begin sampling a water source for its initial survey,
which will eventually result in a MWQP.
We note that this issue was addressed in the 2016 final rule that
extended and clarified compliance dates for certain FSMA provisions (81
FR 57784 at 57793-94). However, we recognize that there is still
confusion about when the MWQP must be completed under the simplified
compliance date structure we are finalizing here. We are therefore
clarifying that farms are not required to have already developed a
completed MWQP as of their new compliance date. Rather, farms must
begin sampling and testing their untreated water sources in accordance
with Sec. 112.46(b)(1), as applicable, by their compliance date. If
the compliance date is not an appropriate time to engage in the
relevant sampling and testing activities--for example, because of the
requirement in Sec. 112.46(b)(1)(ii) that samples be representative of
your use of the water--then compliance must begin by the first relevant
time period that occurs after the compliance date.
To elaborate on what this would mean in practical terms, for a farm
that is not small or very small, compliance must begin by the first
relevant time period that occurs on or after January 26, 2022.
[[Page 9712]]
For example, if a farm that is not small or very small only uses an
untreated water source for agricultural water in May, a compliance date
of January 26, 2022, would indicate that sample collection under Sec.
112.46(b)(1) must take place in May 2022, as that is the time in which
water samples collected would be representative of their use of the
water. Farms that wish to develop or begin developing their MWQP prior
to their compliance date are welcome to do so; but in the above
example, FDA would not expect sample collection to have begun prior to
May 2022.
To provide a few examples related to the number and timing of
samples, all of the following possible approaches are acceptable for
farms that are not small or very small:
Beginning in 2022, conducting an initial survey of an
untreated surface water source by taking 10 samples per year over 2
years (10 in 2022 and 10 in 2023) for a total of 20 samples in
accordance with Sec. 112.46(b)(1)(i)(A); calculating the MWQP for the
first time upon completing the 20-sample data set in 2023; and applying
any necessary corrective actions under Sec. 112.45(b) as soon as
practicable and no later than the following year (e.g., during the 2024
growing season).
Beginning in 2022, conducting an initial survey of an
untreated surface water source by taking 5 samples per year over 4
years (5 in 2022, 5 in 2023, 5 in 2024, and 5 in 2025) for a total of
20 samples, in accordance with Sec. 112.46(b)(1)(i)(A); calculating
the MWQP for the first time upon completing the 20-sample data set in
2025; and applying any necessary corrective actions under Sec.
112.45(b) as soon as practicable and no later than the following year
(e.g., during the 2026 growing season).
Beginning in 2022, conducting an initial survey of an
untreated ground water source by taking 4 samples during the 2022
growing season in accordance with Sec. 112.46(b)(1)(i)(B); calculating
the MWQP for the first time upon completing the 4-sample data set at
the end of the 2022 growing season; and applying any necessary
corrective actions under Sec. 112.45(b) as soon as practicable and no
later than the following year (e.g., during the 2023 growing season).
(Comment 7) Some comments requested additional outreach and
education as FDA explores modifications to the agricultural water
testing provisions.
(Response 7) FDA intends to continue to work with an array of
stakeholders to explore and address the concerns around subpart E. As
described above, we will be implementing a rigorous stakeholder
engagement plan over the course of several months. If we determine that
changes to subpart E are necessary, that would require notice and
comment rulemaking and thus the public would have an opportunity to
comment on any proposed changes. If we determine that we can address
concerns through guidance, such a guidance would be considered ``Level
1'' and would be subject to the notice and comment procedures outlined
in Sec. 10.115(g), which is part of FDA's Good Guidance Practices
regulations. We also remain committed to working with covered farms to
prepare for compliance, through outreach, training and education, and
other collaboration.
(Comment 8) Some comments stated the proposed extension is contrary
to Congress' intent and the plain language of FSMA, noting that the
statute included a deadline for the produce safety final rule.
(Response 8) We do not agree that delaying the compliance date for
subpart E is contrary to Congress's intent or the plain language of the
statute. FSMA required FDA to establish science- and risk-based minimum
standards for the safe production and harvesting of produce for human
consumption (see section 419(a)(1)(A) of the FD&C Act (21 U.S.C.
350h(a)(1)(A))), which we have done by promulgating the produce safety
regulation. Extending the compliance dates for subpart E (for covered
produce other than sprouts) will allow us to evaluate how we can either
improve the requirements or implement them in a way that is less
confusing and more workable for covered farms, in light of the feedback
we have received about subpart E, while still protecting the public
health.
Although FSMA includes deadlines for issuing the proposed and final
rules, there is nothing in the language or spirit of the statute that
is contrary to FDA doing its due diligence to examine how we can
achieve the public health regulatory objectives contained in the rule
in a way that is more practical for covered farms. We reiterate that we
are not changing the compliance dates for the entire produce safety
regulation, just subpart E for covered produce other than sprouts.
(Comment 9) Comments stated that FDA should clearly communicate its
expectations of agricultural water users during the extension.
(Response 9) With this final rule, we are extending the compliance
dates for subpart E of the produce safety regulation for covered
produce other than sprouts. FDA will therefore not expect growers of
covered produce (other than sprouts) to implement subpart E until the
new compliance dates. In the meantime, farms should focus their
attention on good agricultural practices to maintain and protect the
quality of their water sources. (See, e.g., FDA's ``Guide to Minimize
Microbial Food Safety Hazards for Fresh Fruits and Vegetables,'' at
https://www.fda.gov/Food/GuidanceRegulation/GuidanceDocumentsRegulatoryInformation/ucm064574.htm). Farms currently
testing their water may choose to continue with their current water
testing programs, and farms that are not currently testing their water
may choose to begin doing so.
IV. Economic Analysis of Impacts
We have examined the impacts of this rule under Executive Order
12866, Executive Order 13563, Executive Order 13771, the Regulatory
Flexibility Act (5 U.S.C. 601612), and the Unfunded Mandates Reform Act
of 1995 (Pub. L. 104-4). Executive Orders 12866 and 13563 direct us to
assess all costs and benefits of available regulatory alternatives and,
when regulation is necessary, to select regulatory approaches that
maximize net benefits (including potential economic, environmental,
public health and safety, and other advantages; distributive impacts;
and equity). Executive Order 13771 requires that the costs associated
with significant new regulations ``shall, to the extent permitted by
law, be offset by the elimination of existing costs associated with at
least two prior regulations.'' We believe that this final rule is an
economically significant regulatory action as defined by Executive
Order 12866.
The Regulatory Flexibility Act requires Agencies to analyze
regulatory options that will minimize any significant impact of a rule
on small entities. Because this final rule only extends the compliance
dates for certain provisions of the produce safety regulation, we
certify that this final rule will not have a significant economic
impact on a substantial number of small entities.
The Unfunded Mandates Reform Act of 1995 (section 202(a)) requires
us to prepare a written statement, which includes an assessment of
anticipated costs and benefits, before proposing ``any rule that
includes any Federal mandate that may result in the expenditure by
state, local, and tribal governments, in the aggregate, or by the
private sector, of $100,000,000 or more (adjusted annually for
inflation) in any one year.'' The current threshold after
[[Page 9713]]
adjustment for inflation is $150 million, using the most current (2017)
Implicit Price Deflator for the Gross Domestic Product. This final rule
will not result in an expenditure in any year that meets or exceeds
this amount.
This rule extends, for non-sprout covered produce, the compliance
date for all of the provisions of subpart E to 4 years after the
relevant farm's compliance date for all other provisions of the produce
safety regulation (which varies based on establishment size). The
estimated costs and benefits accrued in any given year of compliance
with the produce safety regulation, relative to the first year of
compliance, do not change. However, because the compliance dates for
certain provisions are extended, the discounted value of both total
costs and total benefits decrease.
In the final regulatory impact analysis of subpart E of the produce
safety regulation, we only considered Sec. Sec. 112.42, 112.44,
112.45(a)(2), 112.45(b)(3), 112.46(b), and 112.46(c) to result in a
cost. Therefore, while subpart E has other provisions, only the
aforementioned provisions are relevant to and addressed in this cost
and benefit analysis.
There is a reduction in costs (i.e., cost savings) associated with
extending, for non-sprout covered produce, the compliance date for all
of the provisions of subpart E to 4 years after the relevant farm's
compliance date for the rest of the produce safety regulation. With
respect to their non-sprout covered produce, covered farms have 4 years
from the compliance date for the other provisions of produce safety
regulation to comply with the provisions in subpart E. Thus, while all
initial startup costs and recurring costs remain the same as estimated
in the final regulatory impact analysis for the produce safety
regulation (Ref. 1), the annualized total costs, discounted at 3 (7)
percent over 10 years, decrease from $291 ($265) million to $280 ($254)
million, resulting in a savings of $12 ($10) million.\3\ The present
value of total costs, discounted at 3 (7) percent over 10 years,
decreases from about $2.5 ($1.9) billion to about $2.4 ($1.8) billion,
resulting in a savings of about $99 ($74) million. No additional costs
would be incurred by state, local, and tribal governments or the
private sector as a result of this rule.
---------------------------------------------------------------------------
\3\ The $12 million and $10 million figures are rounded. The
costs decrease from $291.5 ($264.8) million to $279.8 ($254.3)
million, resulting in a savings of $11.6 ($10.5) million.
---------------------------------------------------------------------------
There is a reduction in benefits associated with extending the
compliance dates as described previously. Consumers eating non-sprout
covered produce will not enjoy the potential health benefits (i.e.,
reduced risk of illness) provided by the provisions of subpart E until
2 to 4 years (depending on the specific provision) later than
originally established in the produce safety regulation. Thus, the
annualized total benefits to consumers, discounted at 3 (7) percent
over 10 years, decrease by $104 ($96) million from $800 ($740) million
to $696 ($644) million. The present value of total benefits, discounted
at 3 (7) percent over 10 years, decreases from about $6.8 ($5.2)
billion to about $5.9 ($4.5) billion. Estimated changes in benefits and
costs as a result of this extension are summarized in the following
table.
Table 5--Summary of Changes to Benefits and Costs as a Result of the Final Rule
----------------------------------------------------------------------------------------------------------------
Units
Primary -----------------------------------------------
Category estimate Discount rate
Year dollars (%) Period covered
----------------------------------------------------------------------------------------------------------------
Forgone Benefits:
Annualized.................................. $96 2017 7 2016-2025
Monetized $millions/year.................... 104 2017 3 2016-2025
Forgone Costs:
Annualized.................................. 10 2017 7 2016-2025
Monetized $millions/year.................... 12 2017 3 2016-2025
----------------------------------------------------------------------------------------------------------------
In line with Executive Order 13771, in table 6 we estimate present
and annualized values of costs and cost savings over an infinite time
horizon. Based on these cost-savings, this final rule will be
considered a deregulatory action under Executive Order 13771.
Table 6--Executive Order 13771 Summary Table (in $ Millions 2016
Dollars, Over an Infinite Time Horizon)
------------------------------------------------------------------------
Primary Primary
Item estimate (7%) estimate (3%)
------------------------------------------------------------------------
Present Value of Cost Savings........... $72 $97
Annualized Cost Savings................. 5 3
------------------------------------------------------------------------
We have developed a comprehensive Economic Analysis of Impacts that
assesses the impacts of the final rule. The full analysis of economic
impacts is available in the docket for this rule (Ref. 2) at https://www.regulations.gov, and at https://www.fda.gov/AboutFDA/ReportsManualsForms/Reports/EconomicAnalyses/default.htm.
V. Analysis of Environmental Impact
We have determined under 21 CFR 25.30(j) that this action is of a
type that does not individually or cumulatively have a significant
effect on the human environment. Therefore, neither an environmental
assessment nor an environmental impact statement is required.
VI. Paperwork Reduction Act of 1995
This rule contains no collection of information. Therefore,
clearance by the Office of Management and Budget under the Paperwork
Reduction Act of 1995 is not required.
[[Page 9714]]
VII. Federalism
We have analyzed this rule in accordance with the principles set
forth in Executive Order 13132. FDA has determined that the rule does
not contain policies that have substantial direct effects on the
States, on the relationship between the National Government and the
States, or on the distribution of power and responsibilities among the
various levels of government. Accordingly, we conclude that the rule
does not contain policies that have federalism implications as defined
in the Executive order and, consequently, a federalism summary impact
statement is not required.
VIII. Consultation and Coordination With Indian Tribal Governments
We have analyzed this rule in accordance with the principles set
forth in Executive Order 13175. We have determined that the rule does
not contain policies that have substantial direct effects on one or
more Indian tribes, on the relationship between the Federal Government
and Indian tribes, or on the distribution of power and responsibilities
between the Federal Government and Indian tribes. Accordingly, we
conclude that the rule does not contain policies that have tribal
implications as defined in the Executive order and, consequently, a
tribal summary impact statement is not required.
IX. References
The following references are on display in the Dockets Management
Staff (HFA-305), Food and Drug Administration, 5630 Fishers Lane, Rm.
1061, Rockville, MD 20852 and are available for viewing by interested
persons between 9 a.m. and 4 p.m., Monday through Friday; they are also
available electronically at https://www.regulations.gov. FDA has
verified the website addresses, as of the date this document publishes
in the Federal Register, but websites are subject to change over time.
1. FDA, ``Final Regulatory Impact Analysis, Standards for the
Growing, Harvesting, Packing and Holding of Produce for Human
Consumption.'' November 2015. Available at: https://www.fda.gov/AboutFDA/ReportsManualsForms/Reports/EconomicAnalyses/ucm472310.htm.
2. FDA, ``Final Regulatory Impact Analysis, Final Regulatory
Flexibility Analysis, and Unfunded Mandates Reform Act Analysis for the
Standards for the Growing, Harvesting, Packing, and Holding of Produce
for Human Consumption; Extension of Compliance Dates for Subpart E;
Final Rule,'' 2019. Available at: https://www.fda.gov/AboutFDA/ReportsManualsForms/Reports/EconomicAnalyses/.
Dated: March 6, 2019.
Scott Gottlieb,
Commissioner of Food and Drugs.
[FR Doc. 2019-04652 Filed 3-15-19; 8:45 am]
BILLING CODE 4164-01-P