Akorn, Inc. recalls RIFAMPIN FOR INJECTION USP, 600 mg*/vial, Rx Only. Mfd. for: Akorn, Inc., Lake Forest, IL 60045. NDC: 17478-151-42.
Recalled November 25, 2015 · FDA recall D-0231-2016 · Akorn
Hazard
Failed Impurity/Degradation Specifications: Out of Specifications result obtained for a known impurity. · FDA Class III
Units
6861 Vials
Sold at
US: Nationwide
Description
Failed Impurity/Degradation Specifications: Out of Specifications result obtained for a known impurity.
Product
RIFAMPIN FOR INJECTION USP, 600 mg*/vial, Rx Only. Mfd. for: Akorn, Inc., Lake Forest, IL 60045. NDC: 17478-151-42.
Manufacturer(s)
Akorn, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →