PFIZER INC recalls Vial Label: 8.4% Sodium Bicarbonate Injection, USP, 50mEq/50 mL (1 mEq/mL), Rx only, Hospira, Inc., Lake Forest, IL 6004
Recalled August 27, 2025 · FDA recall D-0591-2025 · PFIZER
Hazard
Lack of Assurance of Sterility. · FDA Class II
Units
15,750 vials
Sold at
U.S. Nationwide
Description
Lack of Assurance of Sterility.
Product
Vial Label: 8.4% Sodium Bicarbonate Injection, USP, 50mEq/50 mL (1 mEq/mL), Rx only, Hospira, Inc., Lake Forest, IL 60045, USA, NDC 0409-6637-24. Case NDC: 00409-6637-14.
Manufacturer(s)
PFIZER INC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →