US Drug Recall Register
Class II · Moderate risk Terminated Initiated Apr 1, 2014 (12 years ago)

Metoprolol Succinate Extended-Release Tablets, USP, 50 mg, 30-count bottle, Rx only…

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

Why it was recalled

Failed Dissolution Specifications: failure of dissolution test observed at nine month time point.

What was recalled

Metoprolol Succinate Extended-Release Tablets, USP, 50 mg, 30-count bottle, Rx only, Manufactured by: Wockhardt Limited, Mumbai, India; Distributed by: Wockhardt USA LLC., 20 Waterview Blvd., Parsippany, NJ 07054, USA; NDC 64679-735-09, UPC 3 64679 73509 1.

Recalling firm
Wockhardt Usa Inc.
NDC code
64679-735-09
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1300-2014

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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