[Congressional Bills 118th Congress]
[From the U.S. Government Publishing Office]
[H.R. 8861 Introduced in House (IH)]
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118th CONGRESS
2d Session
H. R. 8861
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
June 27, 2024
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.
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