# FDA recall D-0009-2015

> **Mylan Pharmaceuticals Inc.** · Class II · drug recall initiated 2014-07-03.

## Product

Metoprolol Succinate Extended-release Tablets, USP 50mg, 90-count Bottles,  Rx only, Mfg by Mylan Pharmaceuticals, Inc. Morgantown, WV  26505. NDC 0378-4596-77.

## Reason for recall

Presence of Foreign Tablets/Capsules: A pharmacist reported a rogue tablet of different size and markings in bottle of Metoprolol

## Distribution

Nationwide

## Key facts

- **Recall number:** D-0009-2015
- **Recalling firm:** Mylan Pharmaceuticals Inc.
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2014-07-03
- **Report date:** 2014-10-15
- **Termination date:** 2016-09-20

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Morgantown, WV, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0009-2015

## Citation

> AI Analytics. FDA recall D-0009-2015. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/D-0009-2015. Source: US FDA. Licensed CC0.

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