Fresenius Kabi USA LLC recalls HALOPERIDOL DECANOATE INJECTION, 50 mg/mL, 1 mL vial, Rx only, Fresenius Kabi USA, LLC, Schaumburg, IL 60173 NDC 63323-
Recalled November 19, 2014 · FDA recall D-0247-2015 · Fresenius Kabi USA
Hazard
Failed Impurities/Degradation Specifications: Fresenius Kabi is recalling three lots of Haloperidol Decanoate Injection due to an out-of-specification result. · FDA Class III
Units
216,517 vials
Sold at
Nationwide and Puerto Rico
Description
Failed Impurities/Degradation Specifications: Fresenius Kabi is recalling three lots of Haloperidol Decanoate Injection due to an out-of-specification result.
Product
HALOPERIDOL DECANOATE INJECTION, 50 mg/mL, 1 mL vial, Rx only, Fresenius Kabi USA, LLC, Schaumburg, IL 60173 NDC 63323-469-01
Manufacturer(s)
Fresenius Kabi USA LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →