Class II

Drug Recall: 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.

PFIZER INC · August 4, 2025

Reason for Recall

Lack of Assurance of Sterility.

Distribution

U.S. Nationwide

States Affected

NATIONWIDE

Quantity Affected

15,750 vials

Source: FDA (openFDA Drug Enforcement)

Recall number: D-0591-2025

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.