# FDA recall D-1702-2012

> **Mylan Pharmaceuticals Inc.** · Class II · drug recall initiated 2012-07-27.

## Product

Levetiracetam Tablets, USP 500 mg, 500 count bottle, Rx only, Manufactured for: Mylan Pharmaceuticals Inc. Morgantown, WV 26505 USA, NDC 0378-5615-05

## Reason for recall

Adulterated Presence of Foreign Tablets: Pharmaceutical manufacturer may have distributed foreign tablets in bottles of Levetiracetam Tablets, USP 500 mg.

## Distribution

The product was distributed to KY.

## Key facts

- **Recall number:** D-1702-2012
- **Recalling firm:** Mylan Pharmaceuticals Inc.
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2012-07-27
- **Report date:** 2012-10-03
- **Termination date:** 2013-05-21

- **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-1702-2012

## Citation

> AI Analytics. FDA recall D-1702-2012. Retrieved 2026-05-25 from https://api.ai-analytics.org/recall/D-1702-2012. Source: US FDA. Licensed CC0.

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