Quinapril Tablets USP — Class III drug recall D-0402-2015
Terminated recall by AVKARE Inc., reported 2015-03-11, distributed nationwide. Subpotent Drug
| Recall number | D-0402-2015 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | AVKARE Inc., Pulaski, TN, United States |
| Recall initiated | 2015-02-27 |
| Classified | 2015-03-04 |
| Reported by FDA | 2015-03-11 |
| Terminated | 2015-09-22 |
| Distributed | Nationwide (US) |
| Quantity | 431 units |
| Reason classes | potency |
| NDC | 50268-0691-15 |
| Lot numbers | I1407932 |
| Expiration dates | 2016-02 |
Product
Quinapril Tablets USP, 40 mg, Rx only, 50 tablets (5 X 10) unit dose pack, Manufactured for: AvKARE, Inc., Pulaski, TN 38478, UPC 5026869115, NDC 50268-691-15
Reason for recall
Subpotent Drug
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-0402-2015. 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.