Akorn, Inc. recalls Ethosuximide Capsules, USP, 250 mg, 100 capsules per bottle, Rx only, Mfg For VersaPharm Incorporated, Maroerre, GA 3006
Recalled September 12, 2018 · FDA recall D-1183-2018 · Akorn
Hazard
Failed Impurities/Degradation Specifications: Out of specification (OOS) results for unspecified impurity. · FDA Class II
Units
23,788 100-count bottles
Sold at
Nationwide in the USA
Description
Failed Impurities/Degradation Specifications: Out of specification (OOS) results for unspecified impurity.
Product
Ethosuximide Capsules, USP, 250 mg, 100 capsules per bottle, Rx only, Mfg For VersaPharm Incorporated, Maroerre, GA 30062. Mfg By: Swiss Caps AG, Kirchberg, Switzerland. NDC: 61748-025-01
Manufacturer(s)
Akorn, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →