US Drug Recall Register
Class II · Moderate risk Terminated Initiated Aug 13, 2018 (8 years ago)

Lisinopril Tablets USP, 10mg, 1000-count bottles, Rx only, Manufactured for: Lupin…

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

Why it was recalled

Presence of Foreign Substance: Product complaint was received of metal contaminant observed in one tablet.

What was recalled

Lisinopril Tablets USP, 10mg, 1000-count bottles, Rx only, Manufactured for: Lupin Pharmaceuticals Inc. Baltimore, Maryland 21202, NDC 68180-980-03

Recalling firm
Lupin Pharmaceuticals Inc.
NDC code
68180-980-03
Origin
MD, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1077-2018

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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