US Drug Recall Register
Class II · Moderate risk Terminated Initiated Jul 3, 2018 (8 years ago)

Metformin Hydrochloride Extended Release Tablets, USP, 500 mg, packaged in a 500-count…

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

Why it was recalled

Presence of foreign substance: One lot fo Metformin Hydrochloride Extended Release Tablets, USP, 500 mg (500 Count) contains foreign matter identified as a piece of rubber glove detected in one tablet.

What was recalled

Metformin Hydrochloride Extended Release Tablets, USP, 500 mg, packaged in a 500-count bottle, Rx only, Distributed by: Sun Pharmaceutical Industries, Inc. Cranbury, NJ 08512, Manufactured by: Sun Pharmaceutical Industries Ltd. Halol-Baroda Highway, Halol-389 350 Gujarat. India, NDC 62756-142-02

Recalling firm
Sun Pharmaceutical Industries, Inc.
NDC code
62756-142-02
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0924-2018

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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