Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Vial Label: 8.4% Sodium Bicarbonate Injection Recalled by PFIZER INC Due to Lack of Assurance of Sterility.
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact PFIZER INC directly.
Affected Products
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.
Quantity: 15,750 vials
Why Was This Recalled?
Lack of Assurance of Sterility.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About PFIZER INC
PFIZER INC has 2 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report