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S.3853 · 119TH CONGRESS

End the Vaccine Carveout Act

Status
In Committee
Latest Action
2026-02-11
Sponsor
Paul, Rand (R-Kentucky)
Official Source
Investability
0/100
Stage
COMMITTEE
Related Bills
1
Full Text
6,078 chars
Alive
Yes

What This Bill Does · Plain English

Summary
Plain-English summary not yet available for this bill. Check back after our next analysis run.

Action Timeline

2026-02-11
Introduced in Senate
2026-02-11
Read twice and referred to the Committee on Health, Education, Labor, and Pensions.

Frequently Asked Questions

Did S.3853 pass?
S.3853 is still alive. Current stage: COMMITTEE. Pass likelihood: pending.
Who sponsored S.3853?
S.3853 was sponsored by Rand Paul (R-Kentucky).

Full Bill Text

119 S3853 IS: End the Vaccine Carveout Act U.S. Senate 2026-02-11 text/xml EN Pursuant to Title 17 Section 105 of the United States Code, this file is not subject to copyright protection and is in the public domain. II 119th CONGRESS 2d Session S. 3853 IN THE SENATE OF THE UNITED STATES February 11, 2026 Mr. Paul (for himself and Mr. Lee ) introduced the following bill; which was read twice and referred to the Committee on Health, Education, Labor, and Pensions A BILL To amend the Public Health Service Act to end the liability shield for vaccine manufacturers, and for other purposes. 1. Short title This Act may be cited as the End the Vaccine Carveout Act . 2. Ending liability shield for vaccine manufacturers (a) National Vaccine Injury Compensation Program (1) Petitions for compensation Section 2111 of the Public Health Service Act ( 42 U.S.C. 300aa–11 ) is amended— (A) in subsection (a)— (i) by striking paragraphs (2), (3), (5), and (6); (ii) by inserting after paragraph (1) the following: (2) Beginning on the date of enactment of the End the Vaccine Carveout Act , and subject to paragraph (4)(B), irrespective of whether a person has filed a petition for compensation under the Program in relation to a vaccine-related injury or death, such person may bring a civil action against a vaccine administrator or manufacturer in a State or Federal court for damages arising from such injury or death. ; (iii) by redesignating paragraph (4) as paragraph (3); (iv) by redesignating paragraphs (7) through (10) as paragraphs (4) through (7), respectively; and (v) by amending paragraph (4) (as so redesignated) to read as follows: (4) (A) If in a civil action brought against a vaccine administrator or manufacturer for a vaccine-related injury or death damages are awarded under a judgment of a court or a settlement of such action, the person who brought such action may not file a petition under subsection (b) for such injury or death, and any pending petition for such injury or death shall be dismissed. (B) If compensation is awarded for a petition filed under the Program for a vaccine-related injury or death, the person who filed such petition may not bring a civil action against a vaccine administrator or manufacturer for such injury or death, and any pending civil action for such injury or death shall be dismissed. ; and (B) in subsection (c)(1)(B)(i)(III), by striking not later than 6 months . (2) Limitations of actions Section 2116(b) of the Public Health Service Act ( 42 U.S.C. 300aa–16(b) ) is amended by striking notwithstanding section 2111(b)(2) and inserting notwithstanding section 2111(b)(2), and unless prohibited by section 2111(a)(4)(A) . (3) Repeals (A) Election Section 2121(a) of the Public Health Service Act ( 42 U.S.C. 300aa–21(a) ) is repealed. (B) Standards of responsibility Section 2122 of the Public Health Service Act ( 42 U.S.C. 300aa–22 ) is repealed. (C) Trial Section 2123 of the Public Health Service Act ( 42 U.S.C. 300aa–23 ) is repealed. (4) Conforming amendments (A) Attorneys’ fees Section 2115(e) of the Public Health Service Act ( 42 U.S.C. 300aa–15(e) ) is amended— (i) by striking paragraph (2); and (ii) by redesignating paragraph (3) as paragraph (2). (B) Payment of compensation Section 2115(f) of the Public Health Service Act ( 42 U.S.C. 300aa–15(f) ) is amended— (i) by striking paragraph (1); (ii) by redesignating paragraphs (2) through (4) as paragraphs (1) through (3), respectively; (iii) in paragraph (1) (as so redesignated), by striking Such compensation may not be paid after an election under section 2121(a) to file a civil action for damages for the vaccine-related injury or death for which such compensation was awarded. ; and (iv) in paragraph (3)(B) (as so redesignated), by striking If the appropriations under subsection (j) are insufficient to make a payment of an annual installment, the limitation on civil actions prescribed by section 2121(a) shall not apply to a civil action for damages brought by the petitioner entitled to the payment. . (C) State limitations of actions Section 2116(c) of the Public Health Service Act ( 42 U.S.C. 300aa–16(c) ) is amended by striking an election is made under section 2121(a) to file the civil action and inserting judgment is entered by the United States Court of Federal Claims (or, if an appeal is taken under section 2112(f), the appellate court’s mandate is issued) with respect to the petition . (D) Termination of program Section 2134(b)(1) of the Public Health Service Act ( 42 U.S.C. 300aa–34(b)(1) ) is amended— (i) by striking and accepted under section 2121(a) ; and (ii) by striking Section 2111(a) and part B shall not apply to civil actions for damages for a vaccine-related injury or death for which a petition may not be filed because of subparagraph (B). . (b) Excluding COVID–19 vaccines from definition of covered countermeasure Section 319F–3(i)(1) of the Public Health Service Act (42 U.S.C. 247d–6d(i)(1)) is amended to read as follows: (1) Covered countermeasure The term covered countermeasure — (A) means— (i) a qualified pandemic or epidemic product (as defined in paragraph (7)); (ii) a security countermeasure (as defined in section 319F–2(c)(1)(B)); (iii) a drug (as such term is defined in section 201(g)(1)) of the Federal Food, Drug, and Cosmetic Act ( 21 U.S.C. 321(g)(1) ), biological product (as such term is defined by section 351(i) of this Act), or device (as such term is defined by section 201(h) of the Federal Food, Drug and Cosmetic Act ( 21 U.S.C. 321(h) )) that is authorized for emergency use in accordance with section 564, 564A, or 564B of the Federal Food, Drug, and Cosmetic Act; or (iv) a respiratory protective device that is approved by the National Institute for Occupational Safety and Health under part 84 of title 42, Code of Federal Regulations (or any successor regulations), and that the Secretary determines to be a priority for use during a public health emergency declared under section 319; and (B) does not include any vaccine used to mitigate, prevent, or treat COVID–19. .
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Bill text sourced from GovInfo.gov · public domain · last updated 2026-10-13. Plain-English summary, score breakdown, and trading-intelligence panels are GovGreed-original analysis derived from STOCK Act filings, SEC Form 4 disclosures, FEC contributions, and Senate LDA lobbying reports — all publicly filed federal records. GovGreed is not affiliated with the U.S. Government. Not financial advice. [live render]