D-1537-2020 Class I Terminated

Recalled by Fresenius Kabi USA, LLC — Lake Zurich, IL

Recall Details

Product Type
Drugs
Report Date
September 2, 2020
Initiation Date
July 22, 2020
Termination Date
September 12, 2022
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
25,100 bottles

Product Description

Dexmedetomidine HCl in 0.9% Sodium Chloride Injection, 200 mcg per 50 mL (4 mcg per mL), for intravenous infusion, preservative free, 50 mL Single Dose Bottle, Rx only, Fresenius Kabi Lake Zurich, IL 60047, NDC 63323-671-05

Reason for Recall

Cross Contamination with other products: trace amounts of lidocaine

Distribution Pattern

U.S.A. Nationwide

Code Information

Lot #: 6121853, Exp 05/2021; 6122207, Exp 06/2021