West-ward Belladonna Alkaloids with Phenobarbital Tablets — Class II drug recall D-824-2013
Terminated recall by West-Ward Pharmaceutical Corp., reported 2013-07-31, distributed nationwide. Presence of Foreign Substance: Belladonna Alkaloids with Phenobarbital Tablets with black specks comprised of
| Recall number | D-824-2013 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | West-Ward Pharmaceutical Corp., Eatontown, NJ, United States |
| Recall initiated | 2013-05-16 |
| Classified | 2013-07-25 |
| Reported by FDA | 2013-07-31 |
| Terminated | 2014-06-23 |
| Distributed | Nationwide (US) |
| Quantity | 14,503 bottles |
| NDC | 00143-1140-10, 00143-1140-51 |
| Lot numbers | 69098A, 69098B, 69100A, 8/15 |
Product
West-ward Belladonna Alkaloids with Phenobarbital Tablets, a) 1000-count bottle (NDC 0143-1140-10), b) 5000-count bottle (NDC 0143-1140-51), Rx only, Manufactured by West-ward Pharmaceutical Corp., Eatontown, N.J., 07724
Reason for recall
Presence of Foreign Substance: Belladonna Alkaloids with Phenobarbital Tablets with black specks comprised of degraded organic material on tablets.
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-824-2013. 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.