Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Ondansetron Injection Recalled by Hospira, Inc. Due to Presence of Particulate; lot being recalled as a...
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
Ondansetron Injection, USP, 4mg/2mL, (2mg/ml), 2mL single-dose Fliptop Vial, Rx only, Sterile, NDC 0409-4755-03, Hospira, Inc, Lake Forest, IL 60045.
Quantity: 340,600 vials
Why Was This Recalled?
Presence of Particulate; lot being recalled as a precaution due to the discovery of 2 particles found in a lot which preceded the recalled lot
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Hospira, Inc.
Hospira, Inc. has 12 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report