# FDA recall D-1541-2014

> **Wockhardt Usa Inc.** · Class II · drug recall initiated 2014-07-24.

## 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 for recall

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

## Distribution

Nationwide

## Key facts

- **Recall number:** D-1541-2014
- **Recalling firm:** Wockhardt Usa Inc.
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2014-07-24
- **Report date:** 2014-08-27
- **Termination date:** 2015-11-20

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Parsippany, NJ, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1541-2014

## Citation

> AI Analytics. FDA recall D-1541-2014. Retrieved 2026-05-27 from https://api.ai-analytics.org/recall/D-1541-2014. Source: US FDA. Licensed CC0.

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