D-0265-2022 Class II Terminated

Recalled by Pfizer Inc. — New York, NY

Recall Details

Product Type
Drugs
Report Date
December 8, 2021
Initiation Date
November 30, 2021
Termination Date
July 12, 2023
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
765 bags

Product Description

5% Dextrose Injection, USP, 50 mL ADD-Vantage Unit, Rx only, Distributed by Hospira, INC., Lake Forest, IL 60045 USA, NDC 0409-7100-68/0409-7100-66

Reason for Recall

Lack of sterility assurance: bag has the potential to leak.

Distribution Pattern

USA Nationwide

Code Information

Lot: 4923608 Exp. 1MAY2022