Pfizer Inc. recalls 4.2% Sodium Bicarbonate Injection, USP 5 mEq/10 mL (0.5 mEq/mL), Glass ABBOJECT Unit of Use Syringe, For Intravenous Use
Recalled January 24, 2024 · FDA recall D-0233-2024 · Pfizer
Hazard
Presence of Particulate Matter; identified as glass · FDA Class I
Units
34000 Cartons
Sold at
Nationwide in the USA and Puerto Rico.
Description
Presence of Particulate Matter; identified as glass
Product
4.2% Sodium Bicarbonate Injection, USP 5 mEq/10 mL (0.5 mEq/mL), Glass ABBOJECT Unit of Use Syringe, For Intravenous Use, Rx Only, 10 mL Syringe per Carton, Hospira, Inc., Lake Forst, IL 60045, NDC 0409-5534-24 (carton), 0409-5534-14 (case).
Manufacturer(s)
Pfizer Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →