# FDA recall D-883-2013

> **West-Ward Pharmaceutical Corp.** · Class II · drug recall initiated 2013-07-30.

## Product

Belladonna Alkaloids with Phenobarbital Tablets, 1000 count (NDC 0143-1140-10) and 5000 count (NDC 0143-1140-51) PET bottles, Rx Only, Manufactured by West-ward Pharmaceutical Corp., Eatontown, N.J., 07724.

## Reason for recall

Presence of Foreign Substance: black specks comprised of degraded organic material found on tablets

## Distribution

Nationwide

## Key facts

- **Recall number:** D-883-2013
- **Recalling firm:** West-Ward Pharmaceutical Corp.
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2013-07-30
- **Report date:** 2013-08-21
- **Termination date:** 2014-06-23

- **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-883-2013

## Citation

> AI Analytics. FDA recall D-883-2013. Retrieved 2026-05-24 from https://api.ai-analytics.org/recall/D-883-2013. Source: US FDA. Licensed CC0.

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