Drug and Device Recall Reporting Act of 1998
Bill journey · stage 2 of 5
Under committee review
What it doesSummary introduced in house (Mar 12, 1998)
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.
What just happenedMar 23, 1998
Referred to the Subcommittee on Health and Environment.
Who’s behind it
- Introduced in HouseMar 12, 1998
- Mar 23, 1998CommitteeH11000
Referred to the Subcommittee on Health and Environment.
Health and Environment Subcommittee - Mar 12, 1998IntroReferralH11100
Referred to the House Committee on Commerce.
Energy and Commerce Committee - Mar 12, 1998IntroReferralIntro-H
Introduced in House
- Mar 12, 1998IntroReferral1000
Introduced in House