Belladonna Alkaloids/PB — Class II drug recall D-826-2013
Terminated recall by Physicians Total Care, Inc., reported 2013-08-07, distributed in GA. Presence of Foriegn Substance:The manufacturer, West-ward Pharmaceutical, recalled product because of the pres
| Recall number | D-826-2013 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Physicians Total Care, Inc., Tulsa, OK, United States |
| Recall initiated | 2013-06-17 |
| Classified | 2013-07-26 |
| Reported by FDA | 2013-08-07 |
| Terminated | 2013-08-15 |
| Distributed | GA |
| Quantity | 270 tablets |
| NDC | 54868-0031-04 |
| Lot numbers | 10/14, 6GP2 |
Product
Belladonna Alkaloids/PB (Belladonna Alkaloids / Phenobarbital) Tablets Phenobarbital USP 16.2 mg, Hyoscyamine Sulfate 0.1037 mg, Atropine Sulfate 0.0194 mg, Scopolamine Hydrobromide 0.0065 mg 30-count bottle (NDC 54868-0031-04), Rx only, Repackaged and distributed by Physicians Total Care, Inc. Tulsa, OK 74146.
Reason for recall
Presence of Foriegn Substance:The manufacturer, West-ward Pharmaceutical, recalled product because of the presence of black spots on tablets. In response, the repackager initiated its own recall.
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-826-2013. 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.