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II
113th CONGRESS
1st Session
S. 541
IN THE SENATE OF THE UNITED STATES
March 12, 2013
Ms. Landrieu (for
herself and Mr. Graham) introduced the
following bill; which was read twice and referred to the
Committee on Health, Education, Labor,
and Pensions
A BILL
To prevent human health threats posed by the consumption
of equines raised in the United States.
1.
Short title
This Act may be cited as the
Safeguard American Food Exports Act of
2013.
2.
Findings
Congress finds that—
(1) unlike cows, pigs,
and other domesticated species, horses and other members of the equidae family
are not raised for the purpose of human consumption;
(2) equines raised in
the United States are frequently treated with substances that are not approved
for use in horses intended for human consumption and equine parts are therefore
unsafe within the meaning of section 409 of the Federal Food, Drug, and
Cosmetic Act;
(3) equines raised in
the United States are frequently treated with drugs, including
phenylbutazone, acepromazine, boldenone undecylenate, omeprazole,
ketoprofen, xylazine, hyaluronic acid, nitrofurazone, polysulfated
glycosaminoglycan, clenbuterol, tolazoline, and ponazuril, which are not
approved for use in horses intended for human consumption and equine parts are
therefore unsafe within the meaning of section 512 of the Federal Food, Drug,
and Cosmetic Act; and
(4) consuming parts of
an equine raised in the United States likely poses a serious threat to human
health and the public should be protected from these unsafe products.
3.
Prohibitions
Section 301 of the Federal Food, Drug, and
Cosmetic Act (21 U.S.C. 331) is amended by adding at the end the
following:
(ccc) Notwithstanding
any other provision of this section—
(1) equine parts
shall be deemed unsafe under section 409 of this Act;
(2) equine parts
shall be deemed unsafe under section 512 of this Act; and
(3) the knowing sale
or transport of equines or equine parts in interstate or foreign commerce for
purposes of human consumption is hereby
prohibited.
.