PlainRecalls
FDA Drug Low Class III Terminated

Haloperidol Decanoate Injection, 50 mg/mL, 1 mL vial, Rx Only. Fresenius Kabi USA LLC, Lake Zurich, IL 60047, NDC 63323-469-01.

Reported: April 20, 2016 Initiated: April 7, 2016 #D-0818-2016

Product Description

Haloperidol Decanoate Injection, 50 mg/mL, 1 mL vial, Rx Only. Fresenius Kabi USA LLC, Lake Zurich, IL 60047, NDC 63323-469-01.

Reason for Recall

Failed Impurities/Degradation Specifications: Firm is recalling product due to an impurity out-of-specification result.

Details

Recalling Firm
Fresenius Kabi USA, LLC
Units Affected
48,210 units
Distribution
Nationwide and Puerto Rico
Location
Lake Zurich, IL

Frequently Asked Questions

What product was recalled?
Haloperidol Decanoate Injection, 50 mg/mL, 1 mL vial, Rx Only. Fresenius Kabi USA LLC, Lake Zurich, IL 60047, NDC 63323-469-01.. Recalled by Fresenius Kabi USA, LLC. Units affected: 48,210 units.
Why was this product recalled?
Failed Impurities/Degradation Specifications: Firm is recalling product due to an impurity out-of-specification result.
Which agency issued this recall?
This recall was issued by the FDA Drug on April 20, 2016. Severity: Low. Recall number: D-0818-2016.