Agency Information Collection (Appeal to Board of Veterans' Appeals) Activity Under OMB Review, 29792-29793 [2015-12369]
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Federal Register / Vol. 80, No. 99 / Friday, May 22, 2015 / Notices
would request from commenters, as part
of such a proceeding.
FOR FURTHER INFORMATION CONTACT:
Arija Flowers, Trial Attorney, Office of
the Chief Counsel, NCC–111, National
Highway Traffic Safety Administration,
1200 New Jersey Avenue SE.,
Washington, DC 20590 (telephone: 202–
366–8714).
SUPPLEMENTARY INFORMATION: In order to
ensure that all vehicles in the United
States are equipped with safe air bags as
quickly as possible and to reduce the
risk of serious injury or death due to an
inflator rupture, NHTSA is considering
exercising its authority under the
National Traffic and Motor Vehicle
Safety Act of 1966, as amended and
recodified (the ‘‘Safety Act’’), 49 U.S.C.
30101, et seq., to organize and prioritize
the remedy programs of BMW of North
America, LLC (‘‘BMW’’), Chrysler
Group, LLC (‘‘Chrysler’’), Daimler
Trucks North America, LLC (‘‘DTNA’’),
Ford Motor Company (‘‘Ford’’), General
Motors, LLC (‘‘GM’’), American Honda
Motor Company (‘‘Honda’’), Mazda
North American Operations (‘‘Mazda’’),
Mitsubishi Motors North America, Inc.
(‘‘Mitsubishi’’), Nissan North America,
Inc. (‘‘Nissan’’), Subaru of America, Inc.
(‘‘Subaru’’), and Toyota Motor
Engineering and Manufacturing
(‘‘Toyota’’) (collectively, the
‘‘Manufacturers’’), and TK Holdings,
Inc. (‘‘Takata’’) to address Takata frontal
air bag inflators. Specifically, NHTSA is
issuing this notice pursuant to its
authority under the Safety Act to
‘‘accelerate’’ a remedy program, 49
U.S.C. 30120(c)(3) and 49 CFR 573.14,
as delegated by the Secretary of
Transportation, 49 CFR 1.95, 501.2(a)(1),
to inspect and investigate, 49 U.S.C.
30166(b)(1), and to ensure that defective
vehicles and equipment are recalled, 49
U.S.C. 30118–30119.
On May 18, 2015, Takata filed four
Defect Information Reports (‘‘DIR’s’’)
pursuant to 49 CFR 573.6. In those
DIR’s, Takata determined that a defect
exists in certain models of frontal air
bag inflators (PSDI, PSDI–4, PSDI–4K,
SPI, PSPI and PSPI–L).
The Safety Act requires manufacturers
to remedy safety-related defects in
motor vehicles. 49 U.S.C. 30120(a). If
the Secretary of Transportation
determines that a manufacturer’s
remedy program is not likely to be
capable of completion within a
reasonable time, the Secretary may
require the manufacturer to ‘‘accelerate’’
the remedy program if the Secretary
finds that there is a risk of serious injury
or death if the remedy program is not
accelerated and that acceleration of the
remedy program can be reasonably
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achieved by expanding the sources of
replacement parts, expanding the
number of authorized repair facilities, or
both. Id. § 30120(c)(3). The Secretary
has delegated his authorities under the
Safety Act to the NHTSA Administrator,
49 CFR 1.95(a), 501.2(a)(1). Each of the
Manufacturers has elected a remedy
program of repair of the affected
vehicles. See 49 U.S.C. 30120(a)(1)(A).
These remedy programs are individual
to each of the Manufacturers, creating a
patch-work solution that NHTSA
believes may not adequately address the
safety risks presented by the defective
Takata inflators within a reasonable
time. Regardless of root cause, these
recalls involve the same safety risk: The
risk of the air bag inflator rupturing
when the air bag is inflated, which may
result in serious injury or death to
vehicle occupants without any prior
warning.
The number of impacted vehicles and
manufacturers in combination with the
supply issues related to these air bag
recalls adds a previously unprecedented
level of complexity to this recall and
remedy process. Given the number of
manufacturers (11) and the technical
complexity of the issues involved,
NHTSA intends to open a Section
30120(c)(3) proceeding, and has
therefore issued this Notice of Intent to
inform the public.
The goal of a Section 30120(c)(3)
proceeding is for the agency to consider
whether (and if so, how) to organize and
prioritize the recall and remedy
programs of the Manufacturers, in order
to aid the Manufacturers in
accomplishing their significant task of
replacing all defective Takata air bag
inflators.
As part of a Section 30120(c)(3)
proceeding, NHTSA plans to consider
the views of commenters regarding
NHTSA’s exercising its authority with
respect to recall and remedy programs
involving certain defective Takata
frontal air bag inflators, including, but
not limited whether it should, and on
what terms, issue an order to
‘‘accelerate’’ all applicable recall
remedy programs, which could include,
but not be limited to, provisions
regarding sourcing, production,
allocation, delivery, installation, and
adequacy of the remedy.
Further, as part of a Section
30120(c)(3) proceeding, NHTSA would
specifically request comments on how
the Manufacturers would comply with
an organization and prioritization of
remedy directive, the possible terms of
any such order and, in particular, how
NHTSA should order the sourcing of the
replacement parts for Manufacturers,
whether NHTSA should issue the
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remedy order to some but not all
Manufacturers, whether NHTSA should
order the Manufacturers to prioritize
certain vehicles or certain regions in its
allocation of replacement parts and
how, and whether NHTSA should order
a re-replacement schedule for
replacement frontal inflators if Takata
cannot provide assurances for the
ongoing safety of the inflators.
Upon NHTSA’s opening of a Section
30120(c)(3) proceeding, additional
information, including how to
comment, will be published in a
supplemental Federal Register Notice.
Authority: 49 U.S.C. 30101, et seq.,
30118–30119, 30120(c)(3), 30166(b)(1); 49
CFR 573.6, 573. 14; delegations of authority
at 49 CFR 1.95(a), 501.2(a)(1).
Issued: May 18, 2015.
Mark R. Rosekind,
Administrator
[FR Doc. 2015–12449 Filed 5–21–15; 8:45 am]
BILLING CODE 4910–59–P
DEPARTMENT OF THE TREASURY
Office of the Comptroller of the
Currency
[OCC Charter Number 706335]
St. James Federal Savings and Loan
Association, St. James, Minnesota;
Approval of Conversion Application
Notice is hereby given that on May 14,
2015, the Office of the Comptroller of
the Currency (OCC) approved the
application of St. James Federal Savings
and Loan Association, St. James,
Minnesota, to convert to the stock form
of organization. Copies of the
application are available for inspection
on the OCC Web site at the FOIA
Electronic Reading Room https://foiapal.occ.gov/palMain.aspx. If you have
any questions, please call OCC
Licensing Activities at (202) 649–6260.
Dated: May 14, 2014.
By the Office of the Comptroller of the
Currency.
Stephen A. Lybarger,
Deputy Comptroller for Licensing.
[FR Doc. 2015–12395 Filed 5–21–15; 8:45 am]
BILLING CODE 4810–33–P
DEPARTMENT OF VETERANS
AFFAIRS
[OMB Control No. 2900–0085]
Agency Information Collection (Appeal
to Board of Veterans’ Appeals) Activity
Under OMB Review
Board of Veterans’ Appeals,
Department of Veterans Affairs.
AGENCY:
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Federal Register / Vol. 80, No. 99 / Friday, May 22, 2015 / Notices
ACTION:
Notice; correction
The Department of Veterans
Affairs (VA) published a collection of
information notice in a Federal Register
February 19, 2015, that contained an
error. The notice incorrectly stated the
agency as ‘‘Office of Acquisition,
Logistics and Construction, Department
of Veterans Affairs.’’ This document
corrects the error by correcting the name
of the agency.
FOR FURTHER INFORMATION CONTACT:
Crystal Rennie, Enterprise Records
Service (005R1B), Department of
Veterans Affairs, 810 Vermont Avenue
NW., Washington, DC 20420, at 202–
632–7492.
SUMMARY:
Correction
In FR Doc. 2015–03425, published on
February 19, 2015, at 80 FR 8952 make
the following correction. On page 8952,
at the top of the page, the name of the
agency should read as follows:
AGENCY: Board of Veterans’ Appeals,
Department of Veterans Affairs.
By direction of the Secretary.
Crystal Rennie,
Department Clearance Officer, Department of
Veterans Affairs.
[FR Doc. 2015–12369 Filed 5–21–15; 8:45 am]
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DEPARTMENT OF VETERANS
AFFAIRS
Research Advisory Committee on Gulf
War Veterans’ Illnesses; Notice of
Meeting
asabaliauskas on DSK5VPTVN1PROD with NOTICES
The Department of Veterans Affairs
(VA) gives notice under the Federal
Advisory Committee Act, 5 U.S.C. App.
2 that the Research Advisory Committee
on Gulf War Veterans’ Illnesses will
meet on June 23, 2015, in Washington,
DC. The meeting will be held in Room
230, 810 Vermont Avenue NW.,
Washington, DC, from 9:00 a.m. until
5:30 p.m. All sessions will be open to
the public. Interested persons who
cannot attend the meeting may use this
toll-free telephone number (800) 767–
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1750; access code 56978# to listen to the
meeting.
The purpose of the Committee is to
provide advice and make
recommendations to the Secretary of
Veterans Affairs on proposed research
studies, research plans, and research
strategies relating to the health
consequences of military service in the
Southwest Asia Theater of operations
during the Gulf War in 1990–1991.
The Committee will review VA
program activities related to Gulf War
Veterans’ Illnesses, and receive updates
on relevant scientific research published
since the last Committee meeting.
Presentations will include updates on
the VA Gulf War Research Program,
followed by research presentations
describing treatments and treatment
research involving Gulf War Veterans.
There will also be a discussion of
Committee business and activities.
The meeting will include time
reserved for public comments in the
afternoon. A sign-up sheet for 5-minute
comments will be available at the
meeting. Individuals who wish to
address the Committee may submit a
1–2 page summary of their comments
for inclusion in the official meeting
record. Members of the public may also
submit written statements for the
Committee’s review to Dr. Roberta
White at rwhite@bu.edu.
Because the meeting is being held in
a Government building, a photo I.D.
must be presented as part of the
clearance process; therefore, any person
attending should allow an additional 15
minutes before the meeting begins. Any
member of the public seeking additional
information should contact Dr. White,
Scientific Director, at (617) 638–4620 or
Dr. Victor Kalasinsky, Designated
Federal Officer, at (202) 443–5682.
Dated: May 19, 2015.
Rebecca Schiller,
Advisory Committee Management Officer.
[FR Doc. 2015–12428 Filed 5–21–15; 8:45 am]
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DEPARTMENT OF VETERANS
AFFAIRS
Genomic Medicine Program Advisory
Committee; Notice of Meeting
The Department of Veterans Affairs
(VA) gives notice under the Federal
Advisory Committee Act, 5 U.S.C. App.
2, that the Genomic Medicine Program
Advisory Committee will meet on June
30, 2015, at the Department of Veterans
Affairs, 810 Vermont Avenue NW.,
Washington, DC 20420, Room 230
(Sonny Montgomery Room). The
meeting will convene at 9:00 a.m. and
adjourn at 5:00 p.m. The meeting is
open to the public.
The purpose of the Committee is to
provide advice and make
recommendations to the Secretary of
Veterans Affairs on using genetic
information to optimize medical care for
Veterans and to enhance development
of tests and treatments for diseases
particularly relevant to Veterans.
The Committee will receive program
updates and continue to provide insight
into optimal ways for VA to incorporate
genomic information into its health care
program while applying appropriate
ethical oversight and protecting the
privacy of Veterans. The meeting focus
will be on developing and
implementing phenotyping and
computational requirements for the
Million Veteran Program. Public
comments will be received at 3:30 p.m.
and are limited to 5 minutes each.
Individuals who speak are invited to
submit a 1–2 page summary of their
comments for inclusion in the official
meeting record to Dr. Sumitra
Muralidhar, Designated Federal Officer,
810 Vermont Avenue NW., Washington,
DC 20420, or by email at
sumitra.muralidhar@va.gov. Any
member of the public seeking additional
information should contact Dr.
Muralidhar at (202) 443–5679.
Dated: May 19, 2015.
Rebecca Schiller,
Committee Management Officer.
[FR Doc. 2015–12511 Filed 5–21–15; 8:45 am]
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Agencies
[Federal Register Volume 80, Number 99 (Friday, May 22, 2015)]
[Notices]
[Pages 29792-29793]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2015-12369]
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DEPARTMENT OF VETERANS AFFAIRS
[OMB Control No. 2900-0085]
Agency Information Collection (Appeal to Board of Veterans'
Appeals) Activity Under OMB Review
AGENCY: Board of Veterans' Appeals, Department of Veterans Affairs.
[[Page 29793]]
ACTION: Notice; correction
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SUMMARY: The Department of Veterans Affairs (VA) published a collection
of information notice in a Federal Register February 19, 2015, that
contained an error. The notice incorrectly stated the agency as
``Office of Acquisition, Logistics and Construction, Department of
Veterans Affairs.'' This document corrects the error by correcting the
name of the agency.
FOR FURTHER INFORMATION CONTACT: Crystal Rennie, Enterprise Records
Service (005R1B), Department of Veterans Affairs, 810 Vermont Avenue
NW., Washington, DC 20420, at 202-632-7492.
Correction
In FR Doc. 2015-03425, published on February 19, 2015, at 80 FR
8952 make the following correction. On page 8952, at the top of the
page, the name of the agency should read as follows:
AGENCY: Board of Veterans' Appeals, Department of Veterans Affairs.
By direction of the Secretary.
Crystal Rennie,
Department Clearance Officer, Department of Veterans Affairs.
[FR Doc. 2015-12369 Filed 5-21-15; 8:45 am]
BILLING CODE 8320-01-P