D-0100-2024 Class I Terminated

Recalled by Pfizer Inc. — New York, NY

Recall Details

Product Type
Drugs
Report Date
November 15, 2023
Initiation Date
October 2, 2023
Termination Date
February 14, 2025
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
24,900 vials

Product Description

4.2% Sodium Bicarbonate Injection, USP 5 mEq/10 mL (0.5mEq/mL), Glass ABBOJECT Unit of Use Syringe, packaged as 1 vial and injector per carton, Rx only, Hospira Inc., Lake Forest, IL 60045, NDC 0409-5534-24

Reason for Recall

Presence of Particulate Matter: identified as glass.

Distribution Pattern

Nationwide in the US and Puerto Rico. The products were not distributed to government accounts or foreign consignees.

Code Information

Lot#: GJ5007, Exp. 8/1/2024