US Drug Recall Register
Class II · Moderate risk Terminated Initiated Sep 15, 2022 (4 years ago)

Lisinopril 10 mg tablets, 30-count Blister Card, Rx Only, MFG: Lupin Pharma, Baltimore…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Presence of Foreign Substance: Foreign material (metal piece) embedded in one tablet.

What was recalled

Lisinopril 10 mg tablets, 30-count Blister Card, Rx Only, MFG: Lupin Pharma, Baltimore, MD Repackaged by: RemedyRepack Inc, Indiana PA. Original NDC# 68180-0980-03, Repackaged NDC# 70518-0468-00

Recalling firm
RemedyRepack Inc.
NDC code
68180-0980-03
Origin
PA, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1538-2022

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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