Aidapak Services, LLC recalls BENAZEPRIL HCL Tablet, 5 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 65162075110

Recalled January 22, 2014 · FDA recall D-712-2014 · Aidapak Services

Hazard

Labeling:Label Mixup; BENAZEPRIL HCL Tablet, 5 mg may be potentially mislabeled as ZINC SULFATE, Capsule, 220 mg, NDC 60258013101, Pedigree: AD52993_34, EXP: 5/20/2014. · FDA Class II

Units

100 Tablets

Sold at

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

Description

Labeling:Label Mixup; BENAZEPRIL HCL Tablet, 5 mg may be potentially mislabeled as ZINC SULFATE, Capsule, 220 mg, NDC 60258013101, Pedigree: AD52993_34, EXP: 5/20/2014.

Product

BENAZEPRIL HCL Tablet, 5 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 65162075110

Manufacturer(s)

Aidapak Services, LLC

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →