# FDA recall D-201-2013

> **West-ward Pharmaceutical Corp.** · Class III · drug recall initiated 2012-11-30.

## Product

Carisoprodol Tablets, USP, 350 mg Rx Only, 100 tablets per bottle, Rx Only, Manufactured by: West-ward Pharmaceutical Corp., Eatontown, NJ 07724, NDC 0143-1176-01.

## Reason for recall

Labeling: Not elsewhere classified: On 12/12/11, DEA published a final rule in the Federal Register making this product a schedule IV (C-IV)controlled substance.  This product is being recalled because this controlled product was not relabeled with the required "C-IV" imprint on the label for products distributed after the 06/11/12 deadline.

## Distribution

Nationwide

## Key facts

- **Recall number:** D-201-2013
- **Recalling firm:** West-ward Pharmaceutical Corp.
- **Classification:** Class III
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2012-11-30
- **Report date:** 2013-03-27
- **Termination date:** 2014-12-18

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-201-2013

## Citation

> AI Analytics. FDA recall D-201-2013. Retrieved 2026-05-25 from https://api.ai-analytics.org/recall/D-201-2013. Source: US FDA. Licensed CC0.

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