D-0105-2021 Class III Terminated

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

Recall Details

Product Type
Drugs
Report Date
December 2, 2020
Initiation Date
November 17, 2020
Termination Date
August 25, 2022
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
16,986 vials

Product Description

DOXOrubicin Hydrochloride Injection, USP, 10 mg / 5 mL (2 mg / mL), 5 mL fill in a 6 mL vial, Single Dose Vial, Rx only, Sterile, Fresenius Kabi, Lake Zurich, IL 60047. NDC: 63323-883-05

Reason for Recall

Cross Contamination with Other Products: trace amounts of octreotide found during testing

Distribution Pattern

Nationwide USA and Puerto Rico

Code Information

Batch: 6120525, exp 11/2020