Aidapak Services, LLC recalls ASCORBIC ACID Tablet, 500 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 60258014101

Recalled January 22, 2014 · FDA recall D-652-2014 · Aidapak Services

Hazard

Labeling:Label Mixup; ASCORBIC ACID Tablet, 500 mg may be potentially mislabeled as FEBUXOSTAT, Tablet, 40 mg, NDC 64764091830, Pedigree: AD23082_16, EXP: 11/1/2013. · FDA Class II

Units

300 Tablets

Sold at

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

Description

Labeling:Label Mixup; ASCORBIC ACID Tablet, 500 mg may be potentially mislabeled as FEBUXOSTAT, Tablet, 40 mg, NDC 64764091830, Pedigree: AD23082_16, EXP: 11/1/2013.

Product

ASCORBIC ACID Tablet, 500 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 60258014101

Manufacturer(s)

Aidapak Services, LLC

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