AVKARE Inc. recalls Quinapril Tablets USP, 5 mg, Rx only, 50 tablets (5 X 10) unit dose pack, Manufactured for: AvKARE, Inc., Pulaski, TN 3…

Recall date

February 27, 2015

Source

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

Recall number

D-0401-2015

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, 5 mg, Rx only, 50 tablets (5 X 10) unit dose pack, Manufactured for: AvKARE, Inc., Pulaski, TN 38478, UPC 5026868815, NDC 50268-688-15