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United States · Bill · S

S. 1767 (105th)

Drug and Device Recall Reporting Act of 1998

referredUnited States· United States Congress· EN

Introduced

16 March 1998

Last action

16 March 1998 · Introduced

Status

Read twice and referred to the Committee on Labor and Human Resources.

Sponsors

Sen. Dodd, Christopher J. [D-CT]

Subjects

Healthcare

Source updated

21 August 2025

Healthcare

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.

This text is taken from the official record. PoliticalRepo does not editorialize.

Timeline

  1. 16 March 1998

    Introduced

    Read twice and referred to the Committee on Labor and Human Resources.

    Source: IntroReferral

  2. 16 March 1998

    Introduced

    Sponsor introductory remarks on measure. (CR S1995)

    Source: IntroReferral

  3. 16 March 1998

    Introduced

    Introduced in Senate

    Source: IntroReferral

Votes

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Versions

Documents

3 official files

Introduced in Senate (text)

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  • Introduced in Senate (text)

    Introduced in Senate · EN · 16 March 1998

    ViewDownloadOpen at official source

  • Introduced in Senate (PDF)

    Introduced in Senate · EN · 16 March 1998

    ViewDownloadOpen at official source

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  • Introduced in Senate

    summary · EN · 16 March 1998

    Open at official source

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Sponsors

Related records

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Sources

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