# FDA recall D-0233-2015

> **Actavis Inc** · Class II · drug recall initiated 2014-08-25.

## Product

Vancomycin Hydrochloride Capsule, USP, 250 mg, 20 count blister pack, Rx Only, Mfd. for: Watson Pharma. Inc. Parsippany, NJ 07054 USA, Mfd. by: Patheon Pharmaceuticals Inc. Cincinnati, OH 45237 USA ---- NDC 0591-3561-15 UPC 3-3-0591356115-1

## Reason for recall

Subpotent Drug

## Distribution

Nationwide

## Key facts

- **Recall number:** D-0233-2015
- **Recalling firm:** Actavis Inc
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2014-08-25
- **Report date:** 2014-11-05
- **Termination date:** 2018-03-21

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0233-2015

## Citation

> AI Analytics. FDA recall D-0233-2015. Retrieved 2026-05-27 from https://api.ai-analytics.org/recall/D-0233-2015. Source: US FDA. Licensed CC0.

---

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