FDAAugust 4, 2025drug

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.

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Lack of Assurance of Sterility.

What to do

FDA enforcement status: Ongoing

Brands named

pfizer

UPCs

00409663714

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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