Class III · Lower riskRecall completed
Quinapril Tablets USP
Unlikely to cause harm — often a labeling or packaging issue.
Does this affect you?
Check your lot numberLot number: I1407932, Exp. 02/2016
Where it was soldNationwide
Find the lot number printed on your box or bottle. If it matches — and you take this medicine — call your pharmacist. Don't stop a prescribed medicine on your own.
What happened
Subpotent Drug
What to do
- Check the lot number and expiry on your medicine against the recall above.
- Talk to your pharmacist or doctor before changing anything — don't stop on your own.
- Report any problems to FDA MedWatch (1-800-FDA-1088 or fda.gov/medwatch).
Who makes it
| Distributed by / for | AvKARE, Inc., Pulaski, TN 38478, UPC 5026869115 |
| NDC | 50268-691-15 |
Show the full FDA record
| Full product label | 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 |
| Recalling firm | AVKARE Inc. |
| Distribution | Nationwide |
| Quantity | 431 unit dose packs |
| Recall initiated | 2015-02-27 |
| Report date | 2015-03-11 |
| Recall completed | 2015-09-22 |
| Recall number | D-0402-2015 |
| Classification | Class III |
| FDA status | Terminated |
| Origin on file | Pulaski TN United States |
Source: U.S. FDA enforcement database (openFDA). Look this up on the official FDA recalls site ↗
This is public FDA recall information, not medical advice. A recall does not always mean your specific bottle is affected. Never stop a prescribed medicine without asking your pharmacist or doctor.