Fresenius Kabi USA, LLC recalls Haloperidol Decanoate Injection, 50 mg/mL, 1 mL vial, Rx Only. Fresenius Kabi USA LLC, Lake Zurich, IL 60047, NDC 63323-
Recalled April 20, 2016 · FDA recall D-0818-2016 · Fresenius Kabi USA
Hazard
Failed Impurities/Degradation Specifications: Firm is recalling product due to an impurity out-of-specification result. · FDA Class III
Units
48,210 units
Sold at
Nationwide and Puerto Rico
Description
Failed Impurities/Degradation Specifications: Firm is recalling product due to an impurity out-of-specification result.
Product
Haloperidol Decanoate Injection, 50 mg/mL, 1 mL vial, Rx Only. Fresenius Kabi USA LLC, Lake Zurich, IL 60047, NDC 63323-469-01.
Manufacturer(s)
Fresenius Kabi USA, LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →