# FDA recall D-189-2013

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

## Product

VERSAPHARM Ethambutol Tablets, USP,400 mg,  Rx Only     a)60 tablets, NDC 61748-014-06, b)90 tablets, NDC 61748-014-09, c)100 tablets, NDC 61748-014-01, d)1000 tablets, NDC 61748-014-10, e) blister pack (10s) 61748-014-11  Manufactured for: VersaPharm Incorporated   Marietta, GA 30062-2260,  Manufactured by: West-ward Pharmaceutical Corp., Eatontown, NJ 07724.

## Reason for recall

Discoloration: Ethambutol Tablets USP 400 mg have tablets cores that may be discolored.

## Distribution

GA

## Key facts

- **Recall number:** D-189-2013
- **Recalling firm:** West-ward Pharmaceutical Corp.
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2012-11-30
- **Report date:** 2013-03-13
- **Termination date:** 2014-01-14

- **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-189-2013

## Citation

> AI Analytics. FDA recall D-189-2013. Retrieved 2026-05-25 from https://api.ai-analytics.org/recall/D-189-2013. Source: US FDA. Licensed CC0.

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