Fresenius Kabi USA, LLC recalls Rifampin for Injection, USP 600mg/vial in a 20mL vial, Rx only, Manufactured for Fresenius Kabi LLC 3 Corporate Drive, L
Recalled July 22, 2015 · FDA recall D-1234-2015 · Fresenius Kabi USA
Hazard
Failed Impurities/Degradation Specifications; out-of-specification for color, impurity, and degradation · FDA Class II
Units
7,593 vials
Sold at
Nationwide,Hawaii, and Puerto Rico
Description
Failed Impurities/Degradation Specifications; out-of-specification for color, impurity, and degradation
Product
Rifampin for Injection, USP 600mg/vial in a 20mL vial, Rx only, Manufactured for Fresenius Kabi LLC 3 Corporate Drive, Lake Zurich, IL, 60047, by Fresenius Kabi LLC, 2020 N Ruby Street, Melrose Park, IL 60160. NDC 63323-351-20
Manufacturer(s)
Fresenius Kabi USA, LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →