Recall D-0591-2025

US Class II Ongoing · initiated 2025-08-04

Recalling firm

PFIZER INC, NY

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.

Reason for recall

Lack of Assurance of Sterility.

← All recalls