Aidapak Services, LLC recalls GLUCOSAMINE/CHONDROITIN Capsule, 500 mg/400 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 54458010022

Recalled January 22, 2014 · FDA recall D-616-2014 · Aidapak Services

Hazard

Labeling:Label Mixup; GLUCOSAMINE/CHONDROITIN Capsule, 500 mg/400 mg may be potentially mislabeled as FEXOFENADINE HCL, Tablet, 60 mg, NDC 45802042578, Pedigree: AD60240_30, EXP: 5/22/2014. · FDA Class II

Units

60 Capsules

Sold at

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

Description

Labeling:Label Mixup; GLUCOSAMINE/CHONDROITIN Capsule, 500 mg/400 mg may be potentially mislabeled as FEXOFENADINE HCL, Tablet, 60 mg, NDC 45802042578, Pedigree: AD60240_30, EXP: 5/22/2014.

Product

GLUCOSAMINE/CHONDROITIN Capsule, 500 mg/400 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 54458010022

Manufacturer(s)

Aidapak Services, LLC

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