US Drug Recall Register
Class II · Moderate risk Terminated Initiated Sep 23, 2020 (6 years ago)

RIOMET ER (metformin hydrochloride for extended-release oral suspension), 500 mg per 5 mL…

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

Why it was recalled

CGMP Deviations: Detection of N-nitrosodimethylamine (NDMA) impurity in finished drug product.

What was recalled

RIOMET ER (metformin hydrochloride for extended-release oral suspension), 500 mg per 5 mL 16 oz. For Oral Use Only Rx Only Manufactured by: Sun Pharmaceuticals Industries Limited Mohali, India Distributed by: Sun Pharmaceuticals Industries, Inc. Cranbury, NJ 08512 NDC 10631-019-17

Recalling firm
Sun Pharmaceutical Industries INC
NDC code
10631-019-17
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0002-2021

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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