VERSAPHARM Ethambutol Tablets — Class II drug recall D-189-2013
Terminated recall by West-ward Pharmaceutical Corp., reported 2013-03-13, distributed in GA. Discoloration: Ethambutol Tablets USP 400 mg have tablets cores that may be discolored.
| Recall number | D-189-2013 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | West-ward Pharmaceutical Corp., Eatontown, NJ, United States |
| Recall initiated | 2012-11-30 |
| Classified | 2013-03-07 |
| Reported by FDA | 2013-03-13 |
| Terminated | 2014-01-14 |
| Distributed | GA |
| Quantity | 18,825 bottles |
| NDC | 61748-0014-01, 61748-0014-06, 61748-0014-09, 61748-0014-10, 61748-0014-11 |
| Expiration dates | 2013-07-20, 2015-07-20 |
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-189-2013. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.