US Drug Recall Register
Class II · Moderate risk Terminated Initiated Sep 13, 2022 (4 years ago)

Lisinopril Tablets USP, 10 mg, 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: Foreign material (metal piece) embedded in one tablet.

What was recalled

Lisinopril Tablets USP, 10 mg, 1000-count bottles, Rx Only, Manufactured for: Lupin Pharmaceuticals, Inc. Baltimore, Maryland 21202, Manufactured by: Lupin Limited, Nagpur- 441 108, India. 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-1536-2022

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.

Other Lisinopril recalls

See all