# FDA recall D-856-2013

> **American Health Packaging** · Class II · drug recall initiated 2013-05-21.

## Product

Zolpidem Tartrate Tablets 5 mg, 10 tablets per blister, 10 blisters per carton, 100 cartons per box, Rx Only, Manufactured for Wockhardt USA LLC., Parsippany, NJ 07054 by Wockhardt Limited, Mumbai, India, NDC 68084-225-01

## Reason for recall

Unit Dose Mispackaging: This recall event is due to a random undetected packaging issue which could increase the potential for a small number of individual unit dose blisters to be packed with more than one tablet.

## Distribution

Nationwide.

## Key facts

- **Recall number:** D-856-2013
- **Recalling firm:** American Health Packaging
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2013-05-21
- **Report date:** 2013-08-14
- **Termination date:** 2013-12-24

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Columbus, OH, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-856-2013

## Citation

> AI Analytics. FDA recall D-856-2013. Retrieved 2026-05-26 from https://api.ai-analytics.org/recall/D-856-2013. Source: US FDA. Licensed CC0.

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*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*
