Perphenazine Tablets — Class II drug recall D-010-2013
Terminated recall by Vintage Pharmaceuticals LLC DBA Qualitest Pharmaceuticals, reported 2012-10-31, distributed nationwide. Tablet Separation: Possibility of cracked or split coating on the tablets.
| Recall number | D-010-2013 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Vintage Pharmaceuticals LLC DBA Qualitest Pharmaceuticals, Huntsville, AL, United States |
| Recall initiated | 2012-10-11 |
| Classified | 2012-10-22 |
| Reported by FDA | 2012-10-31 |
| Terminated | 2013-12-09 |
| Distributed | Nationwide (US) |
| Quantity | 2,755 bottles |
| Reason classes | packaging |
| NDC | 00603-5092-21 |
| Lot numbers | 5/13, C1130511A |
Product
Perphenazine Tablets, USP, 8 mg, 100-count tablets per bottle, Manufactured for: Qualitest Pharmaceuticals, Huntsville, AL 35811, NDC 0603-5092-21.
Reason for recall
Tablet Separation: Possibility of cracked or split coating on the 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-010-2013. 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.