Serious health hazard — there is a reasonable probability that use of or exposure to this product will cause serious adverse health consequences or death.
8.4% Sodium Bicarbonate Injection Recalled by Hospira Inc. Due to Presence of Particulate Matter: particulate matter identified as...
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 Inc. directly.
Affected Products
8.4% Sodium Bicarbonate Injection, USP 50mEq (1mEq/mL), 4.2 grams (84 mg/mL), 50 mL, Rx only, Hospira Inc, Lake Forest, IL 60045, NDC 0409-6625-02
Quantity: 72,000 units
Why Was This Recalled?
Presence of Particulate Matter: particulate matter identified as an insect in one vial.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Hospira Inc.
Hospira Inc. has 245 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report