Medicare and Medicaid Program; Correcting Amendment, 10395-10396 [2014-04024]
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Federal Register / Vol. 79, No. 37 / Tuesday, February 25, 2014 / Rules and Regulations
and adverse human health or
environmental effects of their programs,
policies and activities on minority
populations and low-income
populations in the United States. The
EPA has determined that this final
action will not have disproportionately
high and adverse human health or
environmental effects on minority or
low-income populations because it does
not directly affect the level of protection
provided to human health or the
environment. This rule is making a
finding that Pennsylvania failed to
submit nonattainment SIPs for the 2008
Lead NAAQS as required by the CAA.
The enforceable measures in the
attainment SIPs will ensure that the
areas will attain the NAAQS for lead,
which was established to protect public
health, including the health of minority
and low income populations, with an
adequate margin of safety.
tkelley on DSK3SPTVN1PROD with RULES
K. Congressional Review Act
The Congressional Review Act, 5
U.S.C. 801 et seq., as added by the Small
Business Regulatory Enforcement
Fairness Act of 1996, generally provides
that before a rule may take effect, the
agency promulgating the rule must
submit a rule report, which includes a
copy of the rule, to each House of the
Congress and to the Comptroller General
of the United States. The EPA will
submit a report containing this action
and other required information to the
U.S. Senate, the U.S. House of
Representatives and the Comptroller
General of the United States prior to
publication of the action in the Federal
Register. A major rule cannot take effect
until 60 days after it is published in the
Federal Register. This action is not a
‘‘major rule’’ as defined by 5 U.S.C.
804(2). This action will be effective
February 25, 2014.
L. Judicial Review
Under section 307(b)(1) of the CAA,
petitions for judicial review of this
action must be filed in the United States
Court of Appeals for the Third Circuit
within 60 days from the date this action
is published in the Federal Register.
Filing a petition for reconsideration by
the Administrator of this final action
does not affect the finality of this action
for the purposes of judicial review nor
does it extend the time within which a
petition for judicial review must be
filed, and shall not postpone the
effectiveness of this action.
List of Subjects in 40 CFR Part 52
Environmental protection, Approval
and promulgation of implementation
plans, Administrative practice and
procedures, Air pollution control,
VerDate Mar<15>2010
16:07 Feb 24, 2014
Jkt 232001
Incorporation by reference,
Intergovernmental relations, and
Reporting and recordkeeping
requirements.
Dated: February 7, 2014.
Janet G. McCabe,
Acting Assistant Administrator, Office of Air
and Radiation.
[FR Doc. 2014–03329 Filed 2–24–14; 8:45 am]
BILLING CODE 6560–50–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
42 CFR Part 482
[CMS–3244–F2]
RIN–0938–AQ89
Medicare and Medicaid Program;
Correcting Amendment
Centers for Medicare &
Medicaid Services (CMS), HHS.
ACTION: Final rule; correcting
amendment.
AGENCY:
This document corrects a
technical error that appeared in the final
rule published in the Federal Register
(77 FR 29034) on May 16, 2012, entitled
‘‘Reform of Hospital and Critical Access
Hospital Conditions of Participation.’’
DATES: This correcting amendment is
effective February 25, 2014.
FOR FURTHER INFORMATION CONTACT:
Ronisha Davis, (410) 786–6882.
SUPPLEMENTARY INFORMATION:
SUMMARY:
I. Background
In FR Doc. 2012–11548 (77FR 29034)
of May 16, 2012, the final rule entitled
‘‘Reform of Hospital and Critical Access
Hospital Conditions of Participation,’’
there were technical errors that are
identified and corrected in the
regulations text of this correcting
amendment.
II. Summary of Errors in the
Regulations Text
On page 29075 of the May 16, 2012
Federal Register final rule, in the
amendatory instructions for 42 CFR
482.42, we revised the introductory text
of paragraph (a) to include the
provisions of paragraph (a)(1). However,
we inadvertently neglected to omit
paragraph (a)(1) from the regulations
text. In addition, we proposed to remove
the burdensome requirement for an
infection log at paragraph (a)(2), but
inadvertently omitted the removal of
paragraph (a)(2) from the regulations
text.
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10395
III. Waiver of Proposed Rulemaking
and Delay in Effective Date
We ordinarily publish a notice of
proposed rulemaking in the Federal
Register to provide a period for public
comment before the provisions of a rule
take effect in accordance with section
553(b) of the Administrative Procedure
Act (APA) (5 U.S.C. 553(b)). However,
we can waive this notice and comment
procedure if the Secretary finds, for
good cause, that the notice and
comment process is impracticable,
unnecessary, or contrary to the public
interest, and incorporates a statement of
the finding and the reasons therefore in
the notice.
Section 553(d) of the APA ordinarily
requires a 30-day delay in effective date
of final rules after the date of their
publication in the Federal Register.
This 30-day delay in effective date can
be waived, however, if an agency finds
for good cause that the delay is
impracticable, unnecessary, or contrary
to the public interest, and the agency
incorporates a statement of the findings
and its reasons in the rule issued. The
provision finalized in the final rule
noted above has previously been
subjected to notice and comment
procedures. These corrections do not
make substantive changes to the
requirement that was finalized in the
final rule. In addition, we believe it is
important for the public to have the
correct information as soon as possible
and find no reason to delay the
dissemination of it.
For the reasons stated above, we find
that both notice and comment and the
30-day delay in effective date for the
correction notice are unnecessary.
Therefore, we find there is good cause
to waive notice and comment
procedures and the 30-day delay in
effective date for this correction notice.
List of Subjects in 42 CFR Part 482
Grant programs, Health, Hospitals,
Medicaid, Medicare, Reporting and
recordkeeping requirements.
Accordingly, 42 CFR chapter IV is
corrected by making the following
correcting amendments to part 482:
PART 482—CONDITIONS OF
PARTICIPATION FOR HOSPITALS
1. The authority citation for part 482
continues to read as follows:
■
Authority: Secs. 1102, 1871 and 1881 of
the Social Security Act (42 U.S.C. 1302,
1395hh, and 1395rr), unless otherwise noted.
E:\FR\FM\25FER1.SGM
25FER1
10396
Federal Register / Vol. 79, No. 37 / Tuesday, February 25, 2014 / Rules and Regulations
Subpart C—Basic Hospital Functions
§ 482.42
[Corrected]
2. In § 482.42, remove paragraphs
(a)(1) and (a)(2).
■
(Catalog of Federal Domestic Assistance
Program No. 93.778, Medical Assistance
Program No. 93.773, Medicare—Hospital
Insurance; and Program No. 93.774,
Medicare—Supplementary Medical
Insurance Program)
Dated: February 18, 2014.
Jennifer Cannistra,
Executive Secretary to the Department.
[FR Doc. 2014–04024 Filed 2–24–14; 8:45 am]
BILLING CODE 4120–01–P
DEPARTMENT OF TRANSPORTATION
National Highway Traffic Safety
Administration
49 CFR Part 571
[Docket No. NHTSA–2014–0026]
RIN 2127–AL35
Child Restraint Systems
National Highway Traffic
Safety Administration (NHTSA), U.S.
Department of Transportation (DOT).
ACTION: Final rule; response to petition
for reconsideration.
AGENCY:
This final rule denies most
aspects of a petition for reconsideration
of a February 27, 2012, final rule that
expanded the applicability of the
Federal motor vehicle safety standard
for child restraint systems to child
restraints sold for children weighing up
to 36 kilograms (kg) (80 pounds (lb)).
The petition stated, among other things,
that a label that was required by the
2012 rule for certain child restraints was
unclear and could be misunderstood. In
response, NHTSA is making minor
adjustments to the labeling requirement
to make it clearer and more readerfriendly. For a year, manufacturers have
the option of meeting the requirements
of the February 27, 2012 rule or the rule
as modified today. All other requests for
substantive changes to the 2012 rule are
denied.
DATES: Effective date: The amendments
made by this final rule are effective
February 27, 2014.
Compliance dates: The compliance
date of the amendments of this final rule
is February 27, 2015. Optional early
compliance is permitted. Accordingly,
child restraints manufactured on or after
February 27, 2014 until February 26,
2015, may comply by meeting either the
requirements specified in the February
tkelley on DSK3SPTVN1PROD with RULES
SUMMARY:
VerDate Mar<15>2010
16:07 Feb 24, 2014
Jkt 232001
27, 2012, final rule (77 FR 11626) or
those requirements as amended by
today’s final rule. Child restraints
manufactured on or after February 27,
2015 must meet the requirements as
amended by today’s final rule.
If you wish to petition for
reconsideration of this rule, your
petition must be received by April 11,
2014.
ADDRESSES: If you wish to petition for
reconsideration of this rule, refer in
your petition to the docket number of
this document and submit your petition
to: Administrator, National Highway
Traffic Safety Administration, 1200 New
Jersey Avenue SE., West Building,
Washington, DC 20590. For information
on the Privacy Act, see Rulemaking
Analyses and Notices section.
For access to the docket to read
background documents or comments
received, go to https://
www.regulations.gov and follow the
online instructions for accessing the
docket. You may also visit DOT’s
Docket Management Facility, 1200 New
Jersey Avenue SE., West Building
Ground Floor, Room W12–140,
Washington, DC 20590–0001 for on-line
access to the docket.
FOR FURTHER INFORMATION CONTACT: For
technical issues, you may call Ms.
Cristina Echemendia, Office of
Rulemaking (Telephone: 202–366–6345)
(Fax: 202–493–2990). For legal issues,
you may call Ms. Deirdre Fujita, Office
of Chief Counsel (Telephone: 202–366–
2992) (Fax: 202–366–3820). The mailing
address of the National Highway Traffic
Safety Administration is: 1200 New
Jersey Avenue SE., West Building,
Washington, DC 20590.
SUPPLEMENTARY INFORMATION:
Table of Contents
I. Introduction
II. Petition for Reconsideration
III. Correspondence
a. The Label
b. Other Issues
IV. Agency Response
a. The Label
b. Other Issues
V. Rulemaking Analyses and Notices
I. Introduction
This final rule denies most aspects of
a petition for reconsideration of a
February 27, 2012, final rule (77 FR
11626) that expanded the applicability
of Federal Motor Vehicle Safety
Standard (FMVSS) No. 213, ‘‘Child
restraint systems,’’ from child restraint
systems (CRSs) for children weighing up
to 65 lb to CRSs for children weighing
up to 80 lb. The final rule also adopted
use of a 10-year-old child (10YO) test
dummy (HIII–10C) to test CRSs
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Sfmt 4700
manufactured for children weighing 65
to 80 lb. The test dummy weighs about
78 lb.
Generally speaking, in NHTSA’s
compliance test for FMVSS No. 213,
NHTSA has the choice of assessing the
performance of a CRS when installed on
a bench seat by way of the simulated
lower anchorages of the ‘‘child restraint
anchorage system’’ 1 of the standard seat
assembly or by a seat belt. That is, child
restraint manufacturers must ensure that
their products meet the requirements of
FMVSS No. 213 when NHTSA tests the
CRS attached by the child restraint
anchorage system connectors and when
the agency tests the CRS attached by the
seat belt. During the course of this
particular rulemaking, the Alliance of
Automobile Manufacturers (Alliance)
submitted a comment 2 on an aspect of
the rulemaking proposal relating to how
NHTSA would use the 10YO dummy in
compliance tests, particularly with
respect to an issue concerning attaching
CRSs by the child restraint anchorage
system.3 The Alliance pointed out that
the child restraint anchorage system was
developed by NHTSA to withstand
crash forces in a crash generated by a
mass on the system of 65 lb (mass of
child plus that of CRS).4 Given such a
design parameter, the group stated that
vehicle manufacturers would never
recommend that a CRS be installed
using the vehicle child restraint
anchorage system when used to restrain
1 In 1999, NHTSA issued FMVSS No. 225, ‘‘Child
restraint anchorage systems,’’ which requires
vehicle manufacturers to equip vehicles with child
restraint anchorage systems that are standardized
and independent of the vehicle seat belts. The child
restraint anchorage system required by FMVSS No.
225 is a 3-point system consisting of two lower
anchorage points and an upper anchorage point.
Each lower anchorage consists of a six millimeter
(mm) diameter straight rod, or ‘‘bar,’’ onto which a
CRS connector can be attached. The two lower
anchorage bars are typically located at or near the
seat bight. The upper anchorage (‘‘tether
anchorage’’) is a part to which a tether hook of a
CRS can be attached. The 1999 rule also amended
FMVSS No. 213, ‘‘Child restraint systems,’’ to
require CRSs to be equipped with connectors that
enable the CRS to attach to the vehicle’s lower
anchorages of the child restraint anchorage system.
A new head excursion performance requirement
was added for forward-facing child restraints (other
than booster seats), and to meet it, child restraints
universally use a top tether strap affixed to the top
of the restraints.
2 NHTSA–2007–0048–0008.
3 These are CRSs equipped with an internal
harness (webbing) to restrain the child (‘‘harnessequipped CRSs’’). Forces from the mass of the
child+CRS are imposed on the child restraint
anchorage system. These are not ‘‘belt-positioning
seats’’ used with a vehicle’s Type II seat belt
system.
4 Assuming the mass of the CRS is about 17 lb,
which is approximately the average mass of a CRS,
the child restraint anchorage system is designed for
children weighing up to about 48 lb (for a combined
weight of 65 lb, from the weight of the CRS plus
the weight of the child).
E:\FR\FM\25FER1.SGM
25FER1
Agencies
[Federal Register Volume 79, Number 37 (Tuesday, February 25, 2014)]
[Rules and Regulations]
[Pages 10395-10396]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2014-04024]
=======================================================================
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Medicare & Medicaid Services
42 CFR Part 482
[CMS-3244-F2]
RIN-0938-AQ89
Medicare and Medicaid Program; Correcting Amendment
AGENCY: Centers for Medicare & Medicaid Services (CMS), HHS.
ACTION: Final rule; correcting amendment.
-----------------------------------------------------------------------
SUMMARY: This document corrects a technical error that appeared in the
final rule published in the Federal Register (77 FR 29034) on May 16,
2012, entitled ``Reform of Hospital and Critical Access Hospital
Conditions of Participation.''
DATES: This correcting amendment is effective February 25, 2014.
FOR FURTHER INFORMATION CONTACT: Ronisha Davis, (410) 786-6882.
SUPPLEMENTARY INFORMATION:
I. Background
In FR Doc. 2012-11548 (77FR 29034) of May 16, 2012, the final rule
entitled ``Reform of Hospital and Critical Access Hospital Conditions
of Participation,'' there were technical errors that are identified and
corrected in the regulations text of this correcting amendment.
II. Summary of Errors in the Regulations Text
On page 29075 of the May 16, 2012 Federal Register final rule, in
the amendatory instructions for 42 CFR 482.42, we revised the
introductory text of paragraph (a) to include the provisions of
paragraph (a)(1). However, we inadvertently neglected to omit paragraph
(a)(1) from the regulations text. In addition, we proposed to remove
the burdensome requirement for an infection log at paragraph (a)(2),
but inadvertently omitted the removal of paragraph (a)(2) from the
regulations text.
III. Waiver of Proposed Rulemaking and Delay in Effective Date
We ordinarily publish a notice of proposed rulemaking in the
Federal Register to provide a period for public comment before the
provisions of a rule take effect in accordance with section 553(b) of
the Administrative Procedure Act (APA) (5 U.S.C. 553(b)). However, we
can waive this notice and comment procedure if the Secretary finds, for
good cause, that the notice and comment process is impracticable,
unnecessary, or contrary to the public interest, and incorporates a
statement of the finding and the reasons therefore in the notice.
Section 553(d) of the APA ordinarily requires a 30-day delay in
effective date of final rules after the date of their publication in
the Federal Register. This 30-day delay in effective date can be
waived, however, if an agency finds for good cause that the delay is
impracticable, unnecessary, or contrary to the public interest, and the
agency incorporates a statement of the findings and its reasons in the
rule issued. The provision finalized in the final rule noted above has
previously been subjected to notice and comment procedures. These
corrections do not make substantive changes to the requirement that was
finalized in the final rule. In addition, we believe it is important
for the public to have the correct information as soon as possible and
find no reason to delay the dissemination of it.
For the reasons stated above, we find that both notice and comment
and the 30-day delay in effective date for the correction notice are
unnecessary. Therefore, we find there is good cause to waive notice and
comment procedures and the 30-day delay in effective date for this
correction notice.
List of Subjects in 42 CFR Part 482
Grant programs, Health, Hospitals, Medicaid, Medicare, Reporting
and recordkeeping requirements.
Accordingly, 42 CFR chapter IV is corrected by making the following
correcting amendments to part 482:
PART 482--CONDITIONS OF PARTICIPATION FOR HOSPITALS
0
1. The authority citation for part 482 continues to read as follows:
Authority: Secs. 1102, 1871 and 1881 of the Social Security Act
(42 U.S.C. 1302, 1395hh, and 1395rr), unless otherwise noted.
[[Page 10396]]
Subpart C--Basic Hospital Functions
Sec. 482.42 [Corrected]
0
2. In Sec. 482.42, remove paragraphs (a)(1) and (a)(2).
(Catalog of Federal Domestic Assistance Program No. 93.778, Medical
Assistance Program No. 93.773, Medicare--Hospital Insurance; and
Program No. 93.774, Medicare--Supplementary Medical Insurance
Program)
Dated: February 18, 2014.
Jennifer Cannistra,
Executive Secretary to the Department.
[FR Doc. 2014-04024 Filed 2-24-14; 8:45 am]
BILLING CODE 4120-01-P