Fresenius Kabi USA, LLC recalls Fluphenazine Decanoate Injection, USP; 25 mg/mL, 5mL vials, Rx only, APP Pharmaceuticals, LLC Schaumburg, IL 60173, NDC
Recalled April 12, 2017 · FDA recall D-0647-2017 · Fresenius Kabi USA
Hazard
Subpotent Drug · FDA Class III
Units
118,224 vials
Sold at
Nationwide within the US
Description
Subpotent Drug
Product
Fluphenazine Decanoate Injection, USP; 25 mg/mL, 5mL vials, Rx only, APP Pharmaceuticals, LLC Schaumburg, IL 60173, NDC 63323-0272-05
Manufacturer(s)
Fresenius Kabi USA, LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →