[Congressional Bills 119th Congress] [From the U.S. Government Publishing Office] [H.R. 2715 Introduced in House (IH)]
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119th CONGRESS 1st Session H. R. 2715
To amend the Federal Food, Drug, and Cosmetic Act to extend the destruction authority of the Secretary of Health and Human Services to articles that present a significant public health concern, and for other purposes.
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IN THE HOUSE OF REPRESENTATIVES
April 8, 2025
Mr. Higgins of Louisiana (for himself and Mr. Carter of Louisiana) introduced the following bill; which was referred to the Committee on Energy and Commerce
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A BILL
To amend the Federal Food, Drug, and Cosmetic Act to extend the destruction authority of the Secretary of Health and Human Services to articles that present a significant public health concern, and for other purposes.
Be it enacted by the Senate and House of Representatives of the United States of America in Congress assembled,
SECTION 1. SHORT TITLE.
This Act may be cited as the ``Destruction of Hazardous Imports Act''.
SEC. 2. DESTRUCTION OF CERTAIN REFUSED ARTICLES.
(a) In General.--Section 801(a) of the Federal Food, Drug, and Cosmetic Act (21 U.S.C. 381(a)) is amended-- (1) in the seventh sentence, by striking ``as described under subsection (b).'' and inserting ``as described under subsection (b), or any article refused admission under this section, if the Secretary of Health and Human Services determines that such article presents a significant public health concern.''; and (2) in the eighth, ninth, and tenth sentences, by striking ``drug or device'' each place it appears and inserting ``drug, device, or other article''. (b) Prohibited Acts.--Section 301 of the Federal Food, Drug, and Cosmetic Act (21 U.S.C. 331) is amended by adding at the end the following: ``(jjj) The unauthorized movement, or introduction or delivery for introduction into interstate commerce, including export, of an article that the Secretary has decided to destroy under the seventh sentence of section 801(a).''. (c) Applicability.--The amendments made by subsections (a) and (b) shall apply to articles beginning on the date that is 180 days after the date of enactment of this Act. (d) Regulations.--The Secretary of Health and Human Services, acting through the Commissioner of Food and Drugs, shall-- (1) not later than 90 days after the date of enactment of this Act, finalize such revisions to regulations as may be necessary to implement the amendments made by subsections (a) and (b); and (2) ensure that such regulations are consistent with any applicable international agreements. <all>
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