§ 2102. Ensuring the safety of pet food
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/usc/title-21/section-2102A research copy — for the controlling text, always check the official state or federal source. Not legal advice.
(a)Processing and ingredient standards Not later than 2 years after September 27, 2007, the Secretary of Health and Human Services (referred to in this chapter as the “Secretary”), in consultation with the Association of American Feed Control Officials and other relevant stakeholder groups, including veterinary medical associations, animal health organizations, and pet food manufacturers, shall by regulation establish—
(1)processing standards for pet food; and
(2)updated standards for the labeling of pet food that include nutritional and ingredient information.
(b)Early warning surveillance systems and notification during pet food recalls Not later than 1 year after September 27, 2007, the Secretary shall establish an early warning and surveillance system to identify adulteration of the pet food supply and outbreaks of illness associated with pet food. In establishing such system, the Secretary shall—
(1)consider using surveillance and monitoring mechanisms similar to, or in coordination with, those used to monitor human or animal health, such as the Foodborne Diseases Active Surveillance Network (FoodNet) and PulseNet of the Centers for Disease Control and Prevention, the Food Emergency Response Network of the Food and Drug Administration and the Department of Agriculture, and the National Animal Health Laboratory Network of the Department of Agriculture;
(2)consult with relevant professional associations and private sector veterinary hospitals;
(3)work with the National Companion Animal Surveillance Program, the Health Alert Network, or other notification networks as appropriate to inform veterinarians and relevant stakeholders during any recall of pet food; and
(4)use such information and conduct such other activities as the Secretary deems appropriate.
(Pub. L. 110–85, title X, § 1002, Sept. 27, 2007, 121 Stat. 963; Pub. L. 115–234, title III, § 306(b), Aug. 14, 2018, 132 Stat. 2441.)
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statutes-at-large
- Public Law 110–85To amend the Federal Food, Drug, and Cosmetic Act to revise and extend the user-fee programs for prescription drugs and for medical devices, to enhance the postmarket authorities of the Food and Drug Administration with respect to the safety of drugs, and for other purposes
- Public Law 115–234To amend the Federal Food, Drug, and Cosmetic Act to reauthorize user fee programs relating to new animal drugs and generic new animal drugs
register
- Presidential DocumentsIntroduction to the Unified Agenda of Federal Regulatory and Deregulatory Actions
- NoticesIntroduction to the Regulatory Plan and the Unified Agenda of Federal Regulatory and Deregulatory Actions
- Rules and RegulationsProposed rule
- Rules and RegulationsIntroduction to the Unified Agenda of Federal Regulatory and Deregulatory Actions
statute-compilations
Traces to 2 documents
5 references not yet in our index
- Pub. L. 110–85, title X, § 1002
- 121 Stat. 963
- 132 Stat. 2441
- Pub. L. 110–85
- 121 Stat. 962
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cites case law
§ 2102
Ensuring the safety of pet food
Fed. Reg.×5
Bills×3
Stat.×2
Pub. L.×1
Stat. Comp.×1
Pub. L.Pub. L. 110–85, title X, § 1002
Stat.121 Stat. 963
Stat.132 Stat. 2441
Pub. L.Pub. L. 110–85
Stat.121 Stat. 962
Cites 7Cited by 12 across 5 sources