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Federal Register / Vol. 86, No. 229 / Thursday, December 2, 2021 / Rules and Regulations Is not an economically significant regulatory action based on health or safety risks subject to Executive Order 13045 62 FR 19885, April 23, 1997;
Is not a significant regulatory action subject to Executive Order 13211 66 FR
28355, May 22, 2001;
Is not subject to requirements of section 12d of the National Technology Transfer and Advancement Act of 1995 15 U.S.C. 272 note because application of those requirements would be inconsistent with the CAA; and Does not provide EPA with the discretionary authority to address, as appropriate, disproportionate human health or environmental effects, using practicable and legally permissible methods, under Executive Order 12898
59 FR 7629, February 16, 1994.
The SIP is not approved to apply on any Indian reservation land or in any other area where EPA or an Indian tribe has demonstrated that a tribe has jurisdiction. In those areas of Indian country, the rule does not have tribal implications as specified by Executive Order 13175 65 FR 67249, November 9, 2000, nor will it impose substantial direct costs on tribal governments or preempt tribal law.
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. 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 rule 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. 8042.
Under section 307b1 of the CAA, petitions for judicial review of this action must be filed in the United States Court of Appeals for the appropriate circuit by January 31, 2022. Filing a petition for reconsideration by the Administrator of this final rule 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 may be filed, and shall not postpone the effectiveness of such rule or action. This action may not be challenged later in proceedings to enforce its requirements. See section 307b2.

68423

List of Subjects in 40 CFR Part 52
Environmental Protection, Air Pollution Control, Incorporation by Reference, Intergovernmental Relations, Nitrogen Oxides, Ozone, Reporting and Recordkeeping Requirements, Volatile Organic Compounds.
Dated: November 26, 2021.
John Blevins, Acting Regional Administrator, Region 4.

For the reasons stated in the preamble, EPA amends 40 CFR part 52
as follows:
PART 52APPROVAL AND
PROMULGATION OF
IMPLEMENTATION PLANS
1. The authority citation for part 52
continues to read as follows:

Authority: 42 U.S.C. 7401 et seq.

2. In 52.2220 amend the table in paragraph e by adding, at the end of the table, the entry 1997 8-Hour Ozone Second 10-Year Limited Maintenance Plan for the Montgomery County, Tennessee Area to read as follows:

52.2220

Identification of plan.

e

EPA-APPROVED TENNESSEE NON-REGULATORY PROVISIONS
Name of non-regulatory SIP
provision
Applicable geographic or nonattainment area
State effective date

1997 8-Hour Ozone Second 10Year Limited Maintenance Plan for the Montgomery County, Tennessee Area.

Montgomery County

6/10/2020

FR Doc. 202126143 Filed 12121; 8:45 am BILLING CODE 656050P

DEPARTMENT OF HEALTH AND
HUMAN SERVICES
42 CFR Part 100
RIN 0906AB27

lotter on DSK11XQN23PROD with RULES1

National Vaccine Injury Compensation Program: Adding the Category of Vaccines Recommended for Pregnant Women to the Vaccine Injury Table Health Resources and Services Administration HRSA, Department of Health and Human Services HHS.
ACTION: Final rule.
AGENCY:

On April 4, 2018, the Secretary of Health and Human Services
SUMMARY:

VerDate Sep<11>2014

16:46 Dec 01, 2021

Jkt 256001

EPA approval date

12/2/2021, Insert citation of publication.

the Secretary published in the Federal Register a notice of proposed rulemaking NPRM to amend the National Vaccine Injury Compensation Program VICP or Program Vaccine Injury Table Table, consistent with the statutory requirement to include vaccines recommended by the Centers for Disease Control and Prevention CDC for routine administration in pregnant women. Specifically, the Secretary sought public comment regarding how the addition of this new category should be formatted on the Table. Through this final rule, the Secretary amends the Table to add and/or pregnant women after children to the existing language in Item XVII as proposed in the NPRM.
This change will apply only to petitions for compensation under the VICP filed after the effective date of this final rule.

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Fmt 4700

Explanation
Sfmt 4700

DATES:

This rule is effective January 3,
2022.
FOR FURTHER INFORMATION CONTACT:

Tamara Overby, Acting Director, Division of Injury Compensation Programs, Healthcare Systems Bureau, HRSA, 5600 Fishers Lane, Room 8N146B, Rockville, MD 20857, or by telephone 855 2662427. This is a tollfree number.
SUPPLEMENTARY INFORMATION:
I. Background The National Childhood Vaccine Injury Act of 1986, title III of Public Law 99660 42 U.S.C. 300aa-10 et seq., established the VICP, a Federal compensation program for individuals thought to be injured by certain vaccines. The statute governing the VICP has been amended several times since 1986 and will be hereinafter
E:FRFM02DER1.SGM

02DER1