United States · Bill · HR
H.R. 1108 (115th)
Recall Unsafe Drugs Act of 2017
Introduced
16 February 2017
Last action
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Status
Referred to the Subcommittee on Digital Commerce and Consumer Protection.
Sponsors
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Subjects
Discovery layer
Source updated
11 August 2025
Summary
Recall Unsafe Drugs Act of 2017 This bill amends the Federal Food, Drug, and Cosmetic Act (FFDCA) to require producers of medications to notify the Food and Drug Administration (FDA) of the identity and location of a medication if the producer has reason to believe: (1) that the medication is adulterated or misbranded; and (2) there is a reasonable probability that the use or consumption of, or exposure to, the medication will cause a threat of serious adverse health consequences or death to humans or animals. The FDA may: (1) request that the distributor of a medication that is in violation of the FFDCA voluntarily recall the medication; (2) require the distributor of a medication that may cause serious adverse health consequences to immediately cease distribution of the medication; (3) recall a medication for which distribution has been ceased after giving the distributor an opportunity for an informal hearing; and (4) immediately recall a medication that presents an imminent threat of serious adverse health consequences. Distributors may appeal these FDA orders. In the case of a recall, the FDA must notify consumers and state and local health officials to whom the medication was, or may have been, distributed. Medication distributors must have a recall plan in effect.
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Documents
3 official files
Introduced in House (text)
Introduced in House (text)
Introduced in House · EN · 16 February 2017
Introduced in House (PDF)
Introduced in House · EN · 16 February 2017
Introduced in House
summary · EN · 16 February 2017
Sponsors
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Sources
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- Official source: https://www.congress.gov/bill/115th-congress/house-bill/1108
- Open data entity: https://api.congress.gov/v3/bill/115/hr/1108