Home / Recalls / Pfizer Inc. / D-0136-2020

D-0136-2020 Class II Terminated

Recalled by Pfizer Inc. — New York, NY

Recall Details

Product Type
Drugs
Report Date
October 16, 2019
Initiation Date
October 2, 2019
Termination Date
December 1, 2020
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
17832 bags

Product Description

10% LMD in 5% Dextrose Injection Dextran 40 in Dextrose Injection, USP, 500 mL bags, Rx only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7418-13

Reason for Recall

Lack of Assurance of Sterility: Bag has the potential to leak.

Distribution Pattern

Nationwide in the United States and Puerto Rico

Code Information

Lot #: 87-095-JT Exp. 1MAR2020

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