Substantial Product Hazard Reports, 42028-42031 [E6-11758]
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42028
Federal Register / Vol. 71, No. 142 / Tuesday, July 25, 2006 / Rules and Regulations
the compliance times specified, unless the
actions have already been done.
Service Bulletin References
(f) The term ‘‘service bulletin,’’ as used in
this AD, means the Accomplishment
Instructions of the service bulletin identified
in Table 1 of this AD, as applicable.
TABLE 1.—SERVICE BULLETIN REFERENCES
For Airbus—
And the actions specified in—
Use Airbus Service Bulletin—
Dated—
Model A300 airplanes ..........................
Paragraph
Paragraph
Paragraph
Paragraph
Paragraph
Paragraph
Paragraph
Paragraph
A300–28–0081
A300–28–0079
A310–28–2143
A310–28–2142
A310–28–2153
A300–28–6068
A300–28–6064
A300–28–6077
July 20, 2005.
September 29, 2005.
July 20, 2005.
August 26, 2005.
July 20, 2005.
July 20, 2005.
July 28, 2005.
July 25, 2005.
Model A310 airplanes ..........................
Model A300 B4–601, B4–603, B4–
620, and B4–622 airplanes; Model
A300 B4–605R and B4–622R airplanes; Model A300 F4–605R and
F4–622R airplanes; and Model
A300 C4–605R Variant F airplanes.
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Inspection and Corrective Actions
(g) Within 59 months after the effective
date of this AD: Do a general visual
inspection of the right and left wing fuel
tanks and center fuel tank, if applicable, to
determine if any NSA5516–XXND and
NSA5516–XXNJ type P-clips are installed for
retaining wiring and pipes in any tank, and
do all applicable corrective actions before
further flight after the inspection, by
accomplishing all the actions specified in the
service bulletin.
Note 1: For the purposes of this AD, a
general visual inspection is: ‘‘A visual
examination of an interior or exterior area,
installation, or assembly to detect obvious
damage, failure, or irregularity. This level of
inspection is made from within touching
distance unless otherwise specified. A mirror
may be necessary to ensure visual access to
all surfaces in the inspection area. This level
of inspection is made under normally
available lighting conditions such as
daylight, hangar lighting, flashlight, or
droplight and may require removal or
opening of access panels or doors. Stands,
ladders, or platforms may be required to gain
proximity to the area being checked.’’
Installation of Bonding Leads and Points for
Wing and Center Fuel Tanks
(h) Within 59 months after the effective
date of this AD: Do the actions specified in
paragraphs (h)(1) and (h)(2) of this AD, by
accomplishing all the actions specified in the
service bulletin.
(1) In the center fuel tank, if applicable, do
a general visual inspection of the electrical
bonding points of the equipment identified
in the service bulletin for the presence of a
blue coat, and do all related investigative and
corrective actions before further flight after
the inspection.
(2) In the left and right wing fuel tanks and
center fuel tank, if applicable, install bonding
leads and electrical bonding points on the
equipment identified in the service bulletin.
Installation of Bonding Leads and Points for
the Trim Fuel Tank
(i) For Model A310 airplanes; Model A300
B4–601, B4–603, B4–620, and B4–622
airplanes; Model A300 B4–605R and B4–
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(g) of this AD .....................
(h) of this AD .....................
(g) of this AD .....................
(h) of this AD .....................
(i) of this AD ......................
(g) of this AD .....................
(h) of this AD .....................
(i) of this AD ......................
....................................
....................................
....................................
....................................
....................................
....................................
....................................
....................................
622R airplanes; Model A300 F4–605R and
F4–622R airplanes; and Model A300 C4–
605R Variant F airplanes; equipped with a
trim fuel tank: Within 59 months after the
effective date of this AD, install a new
bonding lead(s) on the water drain system of
the trim fuel tank and install electrical
bonding points on the equipment identified
in the service bulletin in the trim fuel tank,
by accomplishing all the actions specified in
the service bulletin, as applicable.
dms.dot.gov; or at the National Archives and
Records Administration (NARA). For
information on the availability of this
material at the NARA, call (202) 741–6030,
or go to https://www.archives.gov/
federal_register/code_of_federal_regulations/
ibr_locations.html.
Parts Installation
(j) As of the effective date of this AD, no
person may install any NSA5516–XXND or
NSA5516–XXNJ type P-clip for retaining
wiring and pipes in any wing, center, or trim
fuel tank, on any airplane.
Airbus Service
Bulletin—
Alternative Methods of Compliance
(AMOCs)
(k)(1) The Manager, International Branch,
ANM–116, Transport Airplane Directorate,
FAA, has the authority to approve AMOCs
for this AD, if requested in accordance with
the procedures found in 14 CFR 39.19.
(2) Before using any AMOC approved in
accordance with § 39.19 on any airplane to
which the AMOC applies, notify the
appropriate principal inspector in the FAA
Flight Standards Certificate Holding District
Office.
Related Information
(l) French airworthiness directive F–2006–
031, dated February 1, 2006, also addresses
the subject of this AD.
Material Incorporated by Reference
(m) You must use the Airbus service
bulletins identified in Table 2 of this AD to
perform the actions that are required by this
AD, unless the AD specifies otherwise. The
Director of the Federal Register approved the
incorporation by reference of these
documents in accordance with 5 U.S.C.
552(a) and 1 CFR part 51. Contact Airbus, 1
Rond Point Maurice Bellonte, 31707 Blagnac
Cedex, France, for a copy of this service
information. You may review copies at the
Docket Management Facility, U.S.
Department of Transportation, 400 Seventh
Street SW., Room PL–401, Nassif Building,
Washington, DC; on the Internet at https://
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TABLE 2.—MATERIAL INCORPORATED
BY REFERENCE
A300–28–0079
A300–28–0081
A300–28–6064
A300–28–6068
A300–28–6077
A310–28–2142
A310–28–2143
A310–28–2153
Dated—
.........
.........
.........
.........
.........
.........
.........
.........
September 29, 2005.
July 20, 2005.
July 28, 2005.
July 20, 2005.
July 25, 2005.
August 26, 2005.
July 20, 2005.
July 20, 2005.
Issued in Renton, Washington, on July 14,
2006.
Ali Bahrami,
Manager, Transport Airplane Directorate,
Aircraft Certification Service.
[FR Doc. E6–11713 Filed 7–24–06; 8:45 am]
BILLING CODE 4910–13–P
CONSUMER PRODUCT SAFETY
COMMISSION
16 CFR Part 1115
Substantial Product Hazard Reports
Consumer Product Safety
Commission.
AGENCY:
ACTION:
Final interpretative rule.
SUMMARY: Section 15(b) of the Consumer
Product Safety Act, 15 U.S.C. 2064(b),
requires manufacturers, distributors,
and retailers of consumer products to
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report potential product hazards to the
Consumer Product Safety Commission.
On May 26, 2006, the Commission
solicited comments on proposed
revisions to its interpretative rule
advising manufacturers, distributors,
and retailers how to comply with the
requirements of section 15(b). The
proposed revisions identified additional
factors the Commission and staff
consider when assessing whether a
product is defective or not. The
proposed revisions also clarified that
compliance with voluntary or
mandatory product safety standards
may be considered by the Commission
in making certain determinations under
section 15. After considering public
comments, the Commission issues the
accompanying final rule.1
DATES: This final rule becomes effective
on July 25, 2006.
FOR FURTHER INFORMATION CONTACT: John
Gibson Mullan, Assistant Executive
Director, Compliance and Field
Operations at (301) 504–7626.
SUPPLEMENTARY INFORMATION:
A. Background
To provide further guidance, clarity
and transparency on reporting
obligations under section 15(b) of the
Consumer Product Safety Act (CPSA),
15 U.S.C. 2064(b), the Commission, on
May 26, 2006 (71 FR 30350) proposed
revisions to its interpretative rules
regarding reporting of possible
substantial product hazards. Section
15(b) of the CPSA requires that every
manufacturer (including an importer),
distributor or retailer of a consumer
product who obtains information which
reasonably supports the conclusion that
its product fails to comply with an
applicable consumer product safety rule
or with a voluntary consumer product
safety standard upon which the
Commission has relied under section 9
of the CPSA, or contains a defect which
could create a substantial product
hazard as defined in section 15(a)(2) of
the CPSA, or creates an unreasonable
risk of serious injury or death, shall
immediately inform the Commission of
such failure to comply, of such defect,
or of such risk, unless the manufacturer,
distributor or retailer has actual
knowledge that the Commission has
been adequately informed. In 1978, the
Commission first published an
interpretative rule, 16 CFR part 1115,
which explained the section 15(b)
1 The Commission voted 2–1 to issue the final
interpretative rule, Commissioner Thomas Moore
dissenting. Chairman Stratton and Commissioner
Nord filed statements which are available from the
Office of the Secretary or on the Commission’s Web
site at https://www.cpsc.gov.
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15:39 Jul 24, 2006
Jkt 208001
reporting requirement and provided
guidance on filing section 15(b) reports.
In this notice the Commission
finalizes revisions to the interpretative
rule to clarify factors relevant to section
15(b) reporting determinations. These
revisions are not intended to reduce the
number of reports to the Office of
Compliance, to reduce or change the
types of information reported, or to
suggest a diminished need to report.
The Commission received 14
comments in response to the proposed
revisions. Joint comments were
submitted by four ATV companies
(Kawaski Motors Corp., USA; American
Honda Motor Co., Inc.; Polaris
Industries Inc., and Yamaha Motor
Corporation, U.S.A.). Joint comments
were also submitted by four consumer
groups (Consumers Union, Consumer
Federation of America, Kids In Danger,
and U.S. Public Interest Research
Group). Eight commenters supported
the revisions; two of the eight suggested
clarifications to certain provisions. Six
commenters opposed the revisions; five
of the six suggested that the
Commission not adopt the revisions and
one of the six suggested that the
Commission keep the record open. The
Commission received a number of
comments in support of a regulation
related to the assessment of civil
penalties pursuant to section 20 of the
CPSA, 15 U.S.C. 2069(b), (c). A separate
Federal Register notice is being issued
for public comment on this issue.
The Commission received a number
of comments that went beyond the
scope of the proposed revisions. These
included a suggestion for a new appeal
process for preliminary determinations
relating to substantial product hazards,
issues concerning the hazards presented
by counterfeit products, more
widespread notice about the Fast Track
recall process, General Counsel review
of recommendations of proposed
administrative complaints, and
provisions in the adjudicative rules for
joinder and intervention. The
Commission is not incorporating any of
these suggestions since they were not
part of the proposed revisions.
A summary of the comments on the
proposed revisions and our responses
appear below.
B. Section 1115.4 Defect
The first revision clarifies the
Commission’s discussion of ‘‘defect’’ by
adding additional criteria Commission
staff use to evaluate whether a risk of
injury is the type of risk that will render
a product defective, thus possibly
triggering a reporting obligation under
section 15(b). The rule currently states
that in determining whether the risk of
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injury associated with a product is the
type of risk which will render a product
defective, the Commission and staff
consider, as appropriate: the utility of
the product involved; the nature of the
risk of injury which the product
presents; the necessity for the product;
the population exposed to the product
and its risk of injury; the Commission’s
own experience and expertise; the case
law interpreting Federal and State
public health and safety statutes; the
case law in the area of products liability;
and other factors relevant to the
determination. The Commission
proposed to add the following factors as
considerations: the obviousness of such
risk; the adequacy of warnings and
instructions to mitigate such risk; the
role of consumer misuse of the product,
and the foreseeability of such misuse.
The commenters who opposed the
revisions suggested that inclusion of
these additional factors does not clarify
a firm’s reporting obligations but
weakens the intent of the original
regulation by giving firms additional
factors upon which to argue that a
particular product is not defective and
thereby avoid reporting. Several
commenters also suggested that a firm
could rely on just one of the factors—
like consumer misuse—to negate a
reporting obligation.
The Commission’s intent in adopting
this revision is to give further guidance
to firms about reporting defects in their
products. The determination of whether
a product is defective is a threshold
issue in evaluating reporting obligations
under section 15(b) of the CPSA and is
one of the most critical determinations
a company is required to make under
the CPSA. A firm must report if it
obtains information which reasonably
supports the conclusion that a product
it manufactures and/or distributes
contains a defect which could create a
substantial product hazard. 15 U.S.C.
2064(b)(2). The regulatory criteria for
evaluating whether a product presents a
risk of injury that may render it
defective have been in effect since 1978.
In the nearly 30 years since then, the
Commission and staff have evaluated
thousands of products using many
criteria, including, as appropriate, the
criteria now being adopted. The
Commission has concluded, based on
experience and practice in applying the
criteria, that the additional factors—the
obviousness of such risk; the adequacy
of warning and instructions to mitigate
such risk; the role of consumer misuse
of the product and the foreseeability of
such misuse—help clarify the existing
factors in the regulation and enable a
better analysis of whether the risk of
injury associated with a product is the
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type of risk which will render it
defective. This regulation contemplates
consideration of a number of
appropriate factors in making such a
determination. Reliance on one factor
alone cannot negate a reporting
obligation if other factors, as applied,
reasonably support the conclusion that
a defect exists.
The Commission staff already
considers the proposed factors in
making decisions about potential
defects. The current defect regulation
specifies that the Commission and staff
will, as appropriate, consider the case
law in the area of product liability. Two
commenters pointed out that the case
law in the product liability area, as
reflected in the Restatement of Torts,
uses all of the additional criteria
proposed. Thus, the regulation only
makes explicit what was already
implicit in the Commission’s regulation.
C. Section 1115.12(g)(1)(ii) Number of
Defective Products Distributed In
Commerce
The Commission proposed adding the
following statement to an evaluation of
the number of defective products
distributed in commerce when making a
substantial product hazard
determination: ‘‘The Commission also
recognizes that the risk of injury from a
product may decline over time as the
number of products being used by
consumers decreases.’’
Three commenters objected to this
provision. One commenter contended
that the proposed regulatory change is
untrue because the individual risk to a
user from a defective product bears no
relationship to the number of products
in use. Commenters opposed to the
provision also stated that the proposal
gave manufacturers an incentive to wait
to report and to hide problems until a
product is older.
The Commission has clarified the
language of this provision in response to
comments. By this provision, the
Commission is merely recognizing that
the number of products remaining in
consumers hands at any given time is
relevant to a substantial product hazard
determination and that determination
can be influenced by a decline over time
in the number of products remaining in
use. The current regulation can be
misleading because it suggests that the
number of products originally
distributed is the only relevant number
in deciding whether a defective product
presents a substantial risk of injury.
When a potential hazard first appears
long after a product was sold, however,
the more relevant number is not the
number of products originally sold but
the number still with consumers. A firm
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Jkt 208001
may still have a reporting obligation in
such circumstances. The Commission
stresses that firms should never delay
reporting in anticipation of, or because
of, a decrease in the number of products
in use. Firms that delay reporting for
such reasons will be subject to civil
penalties. The final regulation is
reworded to avoid use of the term ‘‘risk’’
which generated some confusion.
D. Section 1115.8 Compliance With
Product Safety Standards
The proposed revisions also add a
new section § 1115.8, ‘‘Compliance with
Product Safety Standards.’’ This section
is intended to further explain how the
Commission views compliance with
applicable voluntary or mandatory
standards, particularly in the context of
decisions under section 15 of the CPSA.
Three of the commenters raised the
objection that this new provision creates
a safe harbor for companies by negating
a reporting obligation when a product
complies with a voluntary or mandatory
standard.
Voluntary Standards. The opposing
commenters mistake the scope and
intent of this provision. It provides no
safe harbor from a reporting obligation.
The text of the rule states that
compliance with voluntary standards
‘‘may be relevant’’ to preliminary
determinations. This language clearly
does not foreclose the possibility that
the staff may make a preliminary
determination that a product presents a
substantial product hazard
notwithstanding compliance with all
applicable voluntary standards.
Although the Commission strongly
supports voluntary standards, such
standards are not always adequate. In
some cases, a defect may involve a
product characteristic or aspect of
performance not addressed by a
standard that is adequate in other
respects, or a product that meets
voluntary standards by design may be
taken out of compliance by a
manufacturing defect. In short, if a
voluntary standard exists and addresses
a product hazard, and the product
complies with such a standard, then
that compliance may be relevant to
considering whether a product
preliminarily presents a substantial
product hazard. Compliance with a
voluntary standard does not preclude a
determination that a substantial product
hazard exists, nor will it relieve a firm
of the requirement to report when a
substantial product hazard may exist.
Firms must not treat compliance with
standards as an excuse not to report.
They should report if a substantial
product hazard may exist and allow the
staff to consider the significance of the
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standard. In the past, the Commission
has sought recalls for products that have
complied with voluntary standards as
well as products that did not comply.
Compliance with an applicable
voluntary standard, as stated in the final
regulation, is merely one factor in this
evaluation.
Mandatory Standards. For reasons
similar to those stated above, the
Commission’s provision for mandatory
standards does not negate a reporting
obligation nor provide safe harbor for
the failure to report. There have been a
number of occasions in the experience
of the Commission staff when a product
is determined to contain a defect that
could create a substantial product
hazard even though such product
complies with a mandatory standard.
The statute and regulations contemplate
a report in such a circumstance. In fact,
reports are especially important in such
cases because they may be the
Commission’s only indication that the
mandatory standards are in need of
revision. At the same time, the
Commission appreciates that it is
generally inappropriate to hold firms to
a higher standard for products
retroactively. As stated in the
regulation, which is slightly reworded
in the final text, compliance with a
mandatory standard should play a role
in the staff’s determination as to
whether a corrective action is necessary.
List of Subjects in 16 CFR Part 1115
Administrative practice and
procedure, Business and Industry,
Consumer protection, Reporting and
recordkeeping requirements.
Accordingly, 16 CFR part 1115 is
amended as follows:
I
PART 1115—SUBSTANTIAL PRODUCT
HAZARD REPORTS
1. The authority citation for part 1115
continues to read as follows:
I
Authority: 15 U.S.C. 2061, 2064, 2065,
2066(a), 2068, 2070, 2071, 2073, 2076, 2079
and 2084.
2. In § 1115.4, amend the concluding
text by adding a new phrase after the
phrase, ‘‘the population exposed to the
product and its risk of injury;’’ to read
as follows:
I
§ 1115.4
Defect.
* * * the obviousness of such risk;
the adequacy of warnings and
instructions to mitigate such risk; the
role of consumer misuse of the product
and the foreseeability of such misuse;’’
* * *
I 3. Section 1115.8 is added to read as
follows:
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§ 1115.8 Compliance with product safety
standards.
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(a) Voluntary standards. The CPSA
and other federal statutes administered
by the Commission generally encourage
the private sector development of, and
compliance with voluntary consumer
product safety standards to help protect
the public from unreasonable risks of
injury associated with consumer
products. To support the development
of such consensus standards,
Commission staff participates in many
voluntary standards committees and
other activities. The Commission also
strongly encourages all firms to comply
with voluntary consumer product safety
standards and considers, where
appropriate, compliance or noncompliance with such standards in
exercising its authorities under the
CPSA and other federal statutes,
including when making determinations
under section 15 of the CPSA. Thus, for
example, whether a product is in
compliance with applicable voluntary
safety standards may be relevant to the
Commission staff’s preliminary
determination of whether that product
presents a substantial product hazard
under section 15 of the CPSA.
(b) Mandatory standards. The CPSA
requires that firms comply with all
applicable mandatory consumer product
safety standards and to report to the
Commission any products which do not
comply with either mandatory
standards or voluntary standards upon
which the Commission has relied. As is
the case with voluntary consumer
product safety standards, compliance or
non-compliance with applicable
mandatory safety standards may be
considered by the Commission and staff
in making relevant determinations and
exercising relevant authorities under the
CPSA and other federal statutes. Thus,
for example, while compliance with a
relevant mandatory product safety
standard does not, of itself, relieve a
firm from the need to report to the
Commission a product defect that
creates a substantial product hazard
under section 15 of the CPSA, it will be
considered by staff in making the
determination of whether and what type
of corrective action may be required.
I 4. Section 1115.12 is amended by
adding a new sentence at the end of
paragraph (g)(1)(ii) to read as follows:
remaining with consumers is a relevant
consideration.
*
*
*
*
*
Dated: July 18, 2006.
Todd A. Stevenson,
Secretary, Consumer Product Safety
Commission.
[FR Doc. E6–11758 Filed 7–24–06; 8:45 am]
BILLING CODE 6355–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
21 CFR Part 101
[Docket No. 2001N–0548] (formerly Docket
No. 01N–0548)
Food Labeling; Guidelines for
Voluntary Nutrition Labeling of Raw
Fruits, Vegetables, and Fish
AGENCY:
ACTION:
Table of Contents
I. Background
II. Comments on the 2002 Proposed Rule and
2005 Reopening of the Comment Period
A. General Comments
B. Consistency Among Government
Agencies in Providing Nutrient
Information
*
*
*
*
*
(g) * * *
(1) * * *
(ii) * * * The Commission also
recognizes that the number of products
15:39 Jul 24, 2006
Jkt 208001
Final rule.
SUMMARY: The Food and Drug
Administration (FDA) is amending the
voluntary nutrition labeling regulations
by updating the names and the nutrition
labeling values for the 20 most
frequently consumed raw fruits,
vegetables, and fish in the United States
and clarifying guidelines for the
voluntary nutrition labeling of these
foods. Availability of the updated
nutrition labeling values in retail stores
and on individually packaged raw
fruits, vegetables, and fish will enable
consumers to make better purchasing
decisions to reflect their dietary needs.
EFFECTIVE DATE: January 1, 2008.
FOR FURTHER INFORMATION CONTACT:
Mary Brandt, Center for Food Safety and
Applied Nutrition (HFS–840), Food and
Drug Administration, 5100 Paint Branch
Pkwy., College Park, MD 20740, 301–
436–1788.
SUPPLEMENTARY INFORMATION:
§ 1115.12 Information which should be
reported; evaluating substantial product
hazard.
VerDate Aug<31>2005
Food and Drug Administration,
HHS.
PO 00000
C. Need for Additional Research and Data
D. Consumer Support for Labeling of Raw
Fruits, Vegetables, and Fish
E. Allowable Nutrient Content Claims
F. Declaration of ‘‘Vitamin A’’ or
‘‘Carotenoid’’
G. Updating of Reference Amounts
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42031
H. Inclusion of Magnesium in Nutrition
Labeling
I. Guidelines for Presentation of the
Nutrition Labeling Values
1. Clarity in Guidelines for Raw Fruits and
Vegetables and for Raw Fish
2. Trans Fatty Acid Labeling
J. Identification of the 20 Most Frequently
Consumed Raw Fruits, Vegetables, and
Fish in the United States
1. Fruits and Vegetables
2. Fish
K. Nutrition Labeling Values for the 20
Most Frequently Consumed Raw Fruits,
Vegetables, and Fish
1. FDA Analysis of Data
a. 95 Percent Prediction Intervals
b. Precision in Estimates
c. Adjusting Values for Total Carbohydrate
2. Nutrition Labeling of Raw Fruits and
Vegetables
a. Apple
b. Avocado
c. Banana
d. Kiwifruit
e. Pear
f. Strawberries
g. Potato
3. Changes to Nutrition Labeling Values
Based Upon Reassessment of 95 Percent
Prediction Intervals
4. Summary of Changes for Fruits and
Vegetables
L. Nutrition Labeling of Raw Fish
M. Effective Date
III. Final Regulatory Impact Analysis
IV. Final Regulatory Flexibility Analysis
V. Unfunded Mandates
VI. Small Business Regulatory Enforcement
Fairness Act of 1996 (SBREFA)
VII. Paperwork Reduction Act of 1995
VIII. Analysis of Environmental Impact
IX. Federalism
X. References
I. Background
In response to requirements of the
Nutrition Labeling and Education Act of
1990 (‘‘the 1990 amendments’’) (Public
Law 101–135), which amended the
Federal Food, Drug, and Cosmetic Act
(the act), FDA (we) published final
regulations in the Federal Register of
November 27, 1991 (56 FR 60880)
(hereinafter identified as ‘‘the 1991 final
rule’’), and corrections in the Federal
Registers of March 6, 1992 (57 FR 8174),
and March 26, 1992 (57 FR 10522), that:
(1) Identified the 20 most frequently
consumed raw fruits, vegetables, and
fish in the United States, which are
those varieties purchased raw but not
necessarily consumed raw; (2)
established guidelines for the voluntary
nutrition labeling of these foods; and (3)
set the criteria for food retailers to meet
substantial compliance with these
guidelines. The 1991 final rule also
required FDA to publish proposed
updates of the nutrition labeling data for
the 20 most frequently consumed raw
fruits, vegetables, and fish (or a notice
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Agencies
[Federal Register Volume 71, Number 142 (Tuesday, July 25, 2006)]
[Rules and Regulations]
[Pages 42028-42031]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E6-11758]
=======================================================================
-----------------------------------------------------------------------
CONSUMER PRODUCT SAFETY COMMISSION
16 CFR Part 1115
Substantial Product Hazard Reports
AGENCY: Consumer Product Safety Commission.
ACTION: Final interpretative rule.
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SUMMARY: Section 15(b) of the Consumer Product Safety Act, 15 U.S.C.
2064(b), requires manufacturers, distributors, and retailers of
consumer products to
[[Page 42029]]
report potential product hazards to the Consumer Product Safety
Commission. On May 26, 2006, the Commission solicited comments on
proposed revisions to its interpretative rule advising manufacturers,
distributors, and retailers how to comply with the requirements of
section 15(b). The proposed revisions identified additional factors the
Commission and staff consider when assessing whether a product is
defective or not. The proposed revisions also clarified that compliance
with voluntary or mandatory product safety standards may be considered
by the Commission in making certain determinations under section 15.
After considering public comments, the Commission issues the
accompanying final rule.\1\
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\1\ The Commission voted 2-1 to issue the final interpretative
rule, Commissioner Thomas Moore dissenting. Chairman Stratton and
Commissioner Nord filed statements which are available from the
Office of the Secretary or on the Commission's Web site at https://
www.cpsc.gov.
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DATES: This final rule becomes effective on July 25, 2006.
FOR FURTHER INFORMATION CONTACT: John Gibson Mullan, Assistant
Executive Director, Compliance and Field Operations at (301) 504-7626.
SUPPLEMENTARY INFORMATION:
A. Background
To provide further guidance, clarity and transparency on reporting
obligations under section 15(b) of the Consumer Product Safety Act
(CPSA), 15 U.S.C. 2064(b), the Commission, on May 26, 2006 (71 FR
30350) proposed revisions to its interpretative rules regarding
reporting of possible substantial product hazards. Section 15(b) of the
CPSA requires that every manufacturer (including an importer),
distributor or retailer of a consumer product who obtains information
which reasonably supports the conclusion that its product fails to
comply with an applicable consumer product safety rule or with a
voluntary consumer product safety standard upon which the Commission
has relied under section 9 of the CPSA, or contains a defect which
could create a substantial product hazard as defined in section
15(a)(2) of the CPSA, or creates an unreasonable risk of serious injury
or death, shall immediately inform the Commission of such failure to
comply, of such defect, or of such risk, unless the manufacturer,
distributor or retailer has actual knowledge that the Commission has
been adequately informed. In 1978, the Commission first published an
interpretative rule, 16 CFR part 1115, which explained the section
15(b) reporting requirement and provided guidance on filing section
15(b) reports.
In this notice the Commission finalizes revisions to the
interpretative rule to clarify factors relevant to section 15(b)
reporting determinations. These revisions are not intended to reduce
the number of reports to the Office of Compliance, to reduce or change
the types of information reported, or to suggest a diminished need to
report.
The Commission received 14 comments in response to the proposed
revisions. Joint comments were submitted by four ATV companies (Kawaski
Motors Corp., USA; American Honda Motor Co., Inc.; Polaris Industries
Inc., and Yamaha Motor Corporation, U.S.A.). Joint comments were also
submitted by four consumer groups (Consumers Union, Consumer Federation
of America, Kids In Danger, and U.S. Public Interest Research Group).
Eight commenters supported the revisions; two of the eight suggested
clarifications to certain provisions. Six commenters opposed the
revisions; five of the six suggested that the Commission not adopt the
revisions and one of the six suggested that the Commission keep the
record open. The Commission received a number of comments in support of
a regulation related to the assessment of civil penalties pursuant to
section 20 of the CPSA, 15 U.S.C. 2069(b), (c). A separate Federal
Register notice is being issued for public comment on this issue.
The Commission received a number of comments that went beyond the
scope of the proposed revisions. These included a suggestion for a new
appeal process for preliminary determinations relating to substantial
product hazards, issues concerning the hazards presented by counterfeit
products, more widespread notice about the Fast Track recall process,
General Counsel review of recommendations of proposed administrative
complaints, and provisions in the adjudicative rules for joinder and
intervention. The Commission is not incorporating any of these
suggestions since they were not part of the proposed revisions.
A summary of the comments on the proposed revisions and our
responses appear below.
B. Section 1115.4 Defect
The first revision clarifies the Commission's discussion of
``defect'' by adding additional criteria Commission staff use to
evaluate whether a risk of injury is the type of risk that will render
a product defective, thus possibly triggering a reporting obligation
under section 15(b). The rule currently states that in determining
whether the risk of injury associated with a product is the type of
risk which will render a product defective, the Commission and staff
consider, as appropriate: the utility of the product involved; the
nature of the risk of injury which the product presents; the necessity
for the product; the population exposed to the product and its risk of
injury; the Commission's own experience and expertise; the case law
interpreting Federal and State public health and safety statutes; the
case law in the area of products liability; and other factors relevant
to the determination. The Commission proposed to add the following
factors as considerations: the obviousness of such risk; the adequacy
of warnings and instructions to mitigate such risk; the role of
consumer misuse of the product, and the foreseeability of such misuse.
The commenters who opposed the revisions suggested that inclusion
of these additional factors does not clarify a firm's reporting
obligations but weakens the intent of the original regulation by giving
firms additional factors upon which to argue that a particular product
is not defective and thereby avoid reporting. Several commenters also
suggested that a firm could rely on just one of the factors--like
consumer misuse--to negate a reporting obligation.
The Commission's intent in adopting this revision is to give
further guidance to firms about reporting defects in their products.
The determination of whether a product is defective is a threshold
issue in evaluating reporting obligations under section 15(b) of the
CPSA and is one of the most critical determinations a company is
required to make under the CPSA. A firm must report if it obtains
information which reasonably supports the conclusion that a product it
manufactures and/or distributes contains a defect which could create a
substantial product hazard. 15 U.S.C. 2064(b)(2). The regulatory
criteria for evaluating whether a product presents a risk of injury
that may render it defective have been in effect since 1978. In the
nearly 30 years since then, the Commission and staff have evaluated
thousands of products using many criteria, including, as appropriate,
the criteria now being adopted. The Commission has concluded, based on
experience and practice in applying the criteria, that the additional
factors--the obviousness of such risk; the adequacy of warning and
instructions to mitigate such risk; the role of consumer misuse of the
product and the foreseeability of such misuse--help clarify the
existing factors in the regulation and enable a better analysis of
whether the risk of injury associated with a product is the
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type of risk which will render it defective. This regulation
contemplates consideration of a number of appropriate factors in making
such a determination. Reliance on one factor alone cannot negate a
reporting obligation if other factors, as applied, reasonably support
the conclusion that a defect exists.
The Commission staff already considers the proposed factors in
making decisions about potential defects. The current defect regulation
specifies that the Commission and staff will, as appropriate, consider
the case law in the area of product liability. Two commenters pointed
out that the case law in the product liability area, as reflected in
the Restatement of Torts, uses all of the additional criteria proposed.
Thus, the regulation only makes explicit what was already implicit in
the Commission's regulation.
C. Section 1115.12(g)(1)(ii) Number of Defective Products Distributed
In Commerce
The Commission proposed adding the following statement to an
evaluation of the number of defective products distributed in commerce
when making a substantial product hazard determination: ``The
Commission also recognizes that the risk of injury from a product may
decline over time as the number of products being used by consumers
decreases.''
Three commenters objected to this provision. One commenter
contended that the proposed regulatory change is untrue because the
individual risk to a user from a defective product bears no
relationship to the number of products in use. Commenters opposed to
the provision also stated that the proposal gave manufacturers an
incentive to wait to report and to hide problems until a product is
older.
The Commission has clarified the language of this provision in
response to comments. By this provision, the Commission is merely
recognizing that the number of products remaining in consumers hands at
any given time is relevant to a substantial product hazard
determination and that determination can be influenced by a decline
over time in the number of products remaining in use. The current
regulation can be misleading because it suggests that the number of
products originally distributed is the only relevant number in deciding
whether a defective product presents a substantial risk of injury. When
a potential hazard first appears long after a product was sold,
however, the more relevant number is not the number of products
originally sold but the number still with consumers. A firm may still
have a reporting obligation in such circumstances. The Commission
stresses that firms should never delay reporting in anticipation of, or
because of, a decrease in the number of products in use. Firms that
delay reporting for such reasons will be subject to civil penalties.
The final regulation is reworded to avoid use of the term ``risk''
which generated some confusion.
D. Section 1115.8 Compliance With Product Safety Standards
The proposed revisions also add a new section Sec. 1115.8,
``Compliance with Product Safety Standards.'' This section is intended
to further explain how the Commission views compliance with applicable
voluntary or mandatory standards, particularly in the context of
decisions under section 15 of the CPSA. Three of the commenters raised
the objection that this new provision creates a safe harbor for
companies by negating a reporting obligation when a product complies
with a voluntary or mandatory standard.
Voluntary Standards. The opposing commenters mistake the scope and
intent of this provision. It provides no safe harbor from a reporting
obligation. The text of the rule states that compliance with voluntary
standards ``may be relevant'' to preliminary determinations. This
language clearly does not foreclose the possibility that the staff may
make a preliminary determination that a product presents a substantial
product hazard notwithstanding compliance with all applicable voluntary
standards. Although the Commission strongly supports voluntary
standards, such standards are not always adequate. In some cases, a
defect may involve a product characteristic or aspect of performance
not addressed by a standard that is adequate in other respects, or a
product that meets voluntary standards by design may be taken out of
compliance by a manufacturing defect. In short, if a voluntary standard
exists and addresses a product hazard, and the product complies with
such a standard, then that compliance may be relevant to considering
whether a product preliminarily presents a substantial product hazard.
Compliance with a voluntary standard does not preclude a determination
that a substantial product hazard exists, nor will it relieve a firm of
the requirement to report when a substantial product hazard may exist.
Firms must not treat compliance with standards as an excuse not to
report. They should report if a substantial product hazard may exist
and allow the staff to consider the significance of the standard. In
the past, the Commission has sought recalls for products that have
complied with voluntary standards as well as products that did not
comply. Compliance with an applicable voluntary standard, as stated in
the final regulation, is merely one factor in this evaluation.
Mandatory Standards. For reasons similar to those stated above, the
Commission's provision for mandatory standards does not negate a
reporting obligation nor provide safe harbor for the failure to report.
There have been a number of occasions in the experience of the
Commission staff when a product is determined to contain a defect that
could create a substantial product hazard even though such product
complies with a mandatory standard. The statute and regulations
contemplate a report in such a circumstance. In fact, reports are
especially important in such cases because they may be the Commission's
only indication that the mandatory standards are in need of revision.
At the same time, the Commission appreciates that it is generally
inappropriate to hold firms to a higher standard for products
retroactively. As stated in the regulation, which is slightly reworded
in the final text, compliance with a mandatory standard should play a
role in the staff's determination as to whether a corrective action is
necessary.
List of Subjects in 16 CFR Part 1115
Administrative practice and procedure, Business and Industry,
Consumer protection, Reporting and recordkeeping requirements.
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Accordingly, 16 CFR part 1115 is amended as follows:
PART 1115--SUBSTANTIAL PRODUCT HAZARD REPORTS
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1. The authority citation for part 1115 continues to read as follows:
Authority: 15 U.S.C. 2061, 2064, 2065, 2066(a), 2068, 2070,
2071, 2073, 2076, 2079 and 2084.
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2. In Sec. 1115.4, amend the concluding text by adding a new phrase
after the phrase, ``the population exposed to the product and its risk
of injury;'' to read as follows:
Sec. 1115.4 Defect.
* * * the obviousness of such risk; the adequacy of warnings and
instructions to mitigate such risk; the role of consumer misuse of the
product and the foreseeability of such misuse;'' * * *
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3. Section 1115.8 is added to read as follows:
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Sec. 1115.8 Compliance with product safety standards.
(a) Voluntary standards. The CPSA and other federal statutes
administered by the Commission generally encourage the private sector
development of, and compliance with voluntary consumer product safety
standards to help protect the public from unreasonable risks of injury
associated with consumer products. To support the development of such
consensus standards, Commission staff participates in many voluntary
standards committees and other activities. The Commission also strongly
encourages all firms to comply with voluntary consumer product safety
standards and considers, where appropriate, compliance or non-
compliance with such standards in exercising its authorities under the
CPSA and other federal statutes, including when making determinations
under section 15 of the CPSA. Thus, for example, whether a product is
in compliance with applicable voluntary safety standards may be
relevant to the Commission staff's preliminary determination of whether
that product presents a substantial product hazard under section 15 of
the CPSA.
(b) Mandatory standards. The CPSA requires that firms comply with
all applicable mandatory consumer product safety standards and to
report to the Commission any products which do not comply with either
mandatory standards or voluntary standards upon which the Commission
has relied. As is the case with voluntary consumer product safety
standards, compliance or non-compliance with applicable mandatory
safety standards may be considered by the Commission and staff in
making relevant determinations and exercising relevant authorities
under the CPSA and other federal statutes. Thus, for example, while
compliance with a relevant mandatory product safety standard does not,
of itself, relieve a firm from the need to report to the Commission a
product defect that creates a substantial product hazard under section
15 of the CPSA, it will be considered by staff in making the
determination of whether and what type of corrective action may be
required.
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4. Section 1115.12 is amended by adding a new sentence at the end of
paragraph (g)(1)(ii) to read as follows:
Sec. 1115.12 Information which should be reported; evaluating
substantial product hazard.
* * * * *
(g) * * *
(1) * * *
(ii) * * * The Commission also recognizes that the number of
products remaining with consumers is a relevant consideration.
* * * * *
Dated: July 18, 2006.
Todd A. Stevenson,
Secretary, Consumer Product Safety Commission.
[FR Doc. E6-11758 Filed 7-24-06; 8:45 am]
BILLING CODE 6355-01-P