Pfizer Inc. recalls 8.4 % Sodium Bicarbonate Injection, USP 50 mEq/50 mL (1 mEq/mL), Lifeshield, Glass ABBOJECT Unit of Use Syringe, Rx Only
Recalled January 24, 2024 · FDA recall D-0234-2024 · Pfizer
Hazard
Presence of Particulate Matter; identified as glass · FDA Class I
Units
21200 Cartons
Sold at
Nationwide in the USA and Puerto Rico.
Description
Presence of Particulate Matter; identified as glass
Product
8.4 % Sodium Bicarbonate Injection, USP 50 mEq/50 mL (1 mEq/mL), Lifeshield, Glass ABBOJECT Unit of Use Syringe, Rx Only, 50 mL Syringe per Carton, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-6637-24 (carton), 0409-6637-14 (case).
Manufacturer(s)
Pfizer Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →