US Drug Recall Register
Class II · Moderate risk Terminated Initiated Feb 22, 2023 (4 years ago)

Metformin hydrochloride Extended-Release Tablets, 1000 mg, 60-count bottle, RX only…

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

Why it was recalled

CGMP Deviations: Detection of N-Nitrosodimethylamine (NDMA) levels in excess of the Acceptable Daily Intake Limit.

What was recalled

Metformin hydrochloride Extended-Release Tablets, 1000 mg, 60-count bottle, RX only, Manufactured by: Actavis Laboratories FL, Inc., Fort Lauderdale, FL 33314 USA, Distributed by: Actavis Pharma, Inc., Parsippany, NJ 07054 USA, NDC 00591-2720-60

Recalling firm
Teva Pharmaceuticals USA Inc
NDC code
00591-2720-60
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0441-2023

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 Chloride recalls

See all