# FDA recall D-220-2013

> **West-ward Pharmaceutical Corp.** · Class II · drug recall initiated 2013-02-06.

## Product

Ciprofloxacin Tablets USP, 500 mg, 100-count bottle, Rx only, Manufactured for West-ward Pharmaceutical Corp., Eatowntown, NJ 07724 by Hikma Pharmaceuticals, Amman, Jordan, NDC 0143-9928-01

## Reason for recall

Presence of Foreign Substance(s): A complaint was received for a rubber-like material in a 500 mg Ciprofloxacin tablet.

## Distribution

GA, AR

## Key facts

- **Recall number:** D-220-2013
- **Recalling firm:** West-ward Pharmaceutical Corp.
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2013-02-06
- **Report date:** 2013-04-03
- **Termination date:** 2014-08-04

- **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-220-2013

## Citation

> AI Analytics. FDA recall D-220-2013. Retrieved 2026-05-26 from https://api.ai-analytics.org/recall/D-220-2013. Source: US FDA. Licensed CC0.

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