Lisinopril Tablets — Class II drug recall D-1406-2015
Terminated recall by Vintage Pharmaceuticals LLC dba Qualitest Pharmaceuticals, reported 2015-09-09, distributed nationwide. Failed Dissolution Specifications
| Recall number | D-1406-2015 |
|---|---|
| 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 | 2015-07-29 |
| Classified | 2015-09-01 |
| Reported by FDA | 2015-09-09 |
| Terminated | 2016-03-29 |
| Distributed | Nationwide (US) |
| Quantity | 8,705 bottles |
| Reason classes | specification failure |
| NDC | 00603-4214-28, 00603-4214-60 |
Product
Lisinopril Tablets, USP, 40 mg, a) 45-count bottle (NDC 0603-4214-60), b) 500-count bottle (NDC 0603-4214-28), Rx Only, Manufactured for: Qualitest Pharmaceuticals, Huntsville, AL 35811
Reason for recall
Failed Dissolution Specifications
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-1406-2015. 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.