United States · Bill · S
S. 1767 (105th)
Drug and Device Recall Reporting Act of 1998
Introduced
16 March 1998
Last action
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Status
Read twice and referred to the Committee on Labor and Human Resources.
Sponsors
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Subjects
Discovery layer
Source updated
21 August 2025
Summary
Drug and Device Recall Reporting Act of 1998 - Amends the Federal Food, Drug, and Cosmetic Act to require a pharmacy that receives notice from a recalling firm of a Class I or Class II recall of a drug or device to notify retail customers that received the drug or device: (1) in writing, for customers receiving the drug or device on prescription; and (2) by public display, for all others. Mandates a civil monetary penalty for violations.
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Timeline
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Votes
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Versions
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Documents
3 official files
Introduced in Senate (text)
Introduced in Senate (text)
Introduced in Senate · EN · 16 March 1998
Introduced in Senate (PDF)
Introduced in Senate · EN · 16 March 1998
Introduced in Senate
summary · EN · 16 March 1998
Sponsors
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Related records
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Sources
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- Official source: https://www.congress.gov/bill/105th-congress/senate-bill/1767
- Open data entity: https://api.congress.gov/v3/bill/105/s/1767