Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Furosemide Injection USP (10 mg/mL) Recalled by Hospira, Inc. Due to Lack of Assurance of Sterility; possible loose crimp...
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
Furosemide Injection USP (10 mg/mL), 4 mL in 5 mL Fliptop Vial, Rx only, Hospira Inc., Lake Forest, IL --- NDC 0409-6102-04
Quantity: 63,900 vials
Why Was This Recalled?
Lack of Assurance of Sterility; possible loose crimp applied to fliptop vial
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