Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Neut Sodium Bicarbonate 4% (2.4 mEq) Additive Solution 5 mL Recalled by Hospira a Pfizer Company Due to Lack of Sterility Assurance
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 Hospira a Pfizer Company directly.
Affected Products
Neut Sodium Bicarbonate 4% (2.4 mEq) Additive Solution 5 mL , a.) Single-dose vial (NDC 0409-6609-02), b.) 25 vial carton (NDC 0409-6609-25), Rx Only, Mfd by Hospira, INC, Lake Forest, IL 60045 USA
Quantity: 21,436,700 5mL single dose vials
Why Was This Recalled?
Lack of Sterility Assurance
Where Was This Sold?
U.S. (including Puerto Rico), Dutch Antilles, Barbados, Canada, Philippines, Kuwait, and Singapore
About Hospira a Pfizer Company
Hospira a Pfizer Company has 4 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report