Recalls / Class III
Class IIID-0402-2015
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
- Affected lot / code info
- Lot number: I1407932, Exp. 02/2016
Why it was recalled
Subpotent Drug
Recalling firm
- Firm
- AVKARE Inc.
- Notification channel
- Letter
- Type
- Voluntary: Firm initiated
- Address
- 615 N 1st St, N/A, Pulaski, Tennessee 38478-2403
Distribution
- Quantity
- 431 unit dose packs
- Distribution pattern
- Nationwide
Timeline
- Recall initiated
- 2015-02-27
- FDA classified
- 2015-03-04
- Posted by FDA
- 2015-03-11
- Terminated
- 2015-09-22
- Status
- Terminated
Source: openFDA Drug Enforcement endpoint. Recall record D-0402-2015. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.