Fresenius Kabi USA, LLC recalls GENTAMICIN INJECTION, USP, equivalent to 40 mg/mL, Rx only, 20 mL Multiple Dose Vial, Manufactured by APP Pharmaceutical
Recalled December 17, 2014 · FDA recall D-0290-2015 · Fresenius Kabi USA
Hazard
Defective Container: Vials may be missing stoppers. · FDA Class II
Units
92,125 vials
Sold at
Nationwide and Puerto Rico
Description
Defective Container: Vials may be missing stoppers.
Product
GENTAMICIN INJECTION, USP, equivalent to 40 mg/mL, Rx only, 20 mL Multiple Dose Vial, Manufactured by APP Pharmaceuticals, LLC, Schaumburg, IL 60173, NDC 63323-010-20
Manufacturer(s)
Fresenius Kabi USA, LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →