RecallRadar

FDA Drug recall D-1541-2014

Wockhardt Metoprolol Succinate Extended-Release Tablets, USP 200 mg, a) 100-count bottle (NDC 64679-737-02), b) 500-count bottle (NDC 64679…

On 2014-08-27 the FDA classified a Class II recall of Wockhardt Metoprolol Succinate Extended-Release Tablets, USP 200 mg, a) 100-count bottle (NDC 64679-737-02), b) 500-count bottle (NDC 64679… by Wockhardt Usa, citing failed Dissolution Specifications: Dissolution failures found during testing of control samples at the four hour time point.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-1541-2014
ClassificationClass II
Statusterminated
Initiated2014-07-24
Published2014-08-27
Last updated2026-09-13 11:51 UTC
CompanyWockhardt Usa
DistributionUS

Product

Wockhardt Metoprolol Succinate Extended-Release Tablets, USP 200 mg, a) 100-count bottle (NDC 64679-737-02), b) 500-count bottle (NDC 64679-737-03) Rx only, Manufactured by: Wockhardt Limited Mumbai, India Distributed by: Wockhardt USA LLC 20 Waterview Boulevard. Parsippany, NJ 07054 USA

Reason

Failed Dissolution Specifications: Dissolution failures found during testing of control samples at the four hour time point.

Identifiers

code_infoLot # a) LN11005, Exp 04/15; LN11006; Exp 04/15; b) LN10979; Exp. 04/15, LN10980; Exp. 04/15

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1541-2014%22

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