AVKARE Inc. recalls Quinapril Tablets USP, 40 mg, Rx only, 50 tablets (5 X 10) unit dose pack, Manufactured for: AvKARE, Inc., Pulaski, TN…

Recall date

February 27, 2015

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

D-0402-2015

FDA classification

Class III

Brand / firm

AVKARE Inc.

Sold / distributed

Nationwide

Why it was recalled

Subpotent Drug

Class III means the product violates regulations but is not likely to cause harm.

What was recalled

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