Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Vancomycin Hydrochloride for Injection Recalled by Hospira Inc. Due to Temperature Abuse: Products experienced uncontrolled temperature excursions during...
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
Vancomycin Hydrochloride for Injection, USP, 500 mg Sterile Powder per Fliptop Vial, packaged in 10 Units per carton, Rx only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-4332-01.
Quantity: 200 vials
Why Was This Recalled?
Temperature Abuse: Products experienced uncontrolled temperature excursions during transit.
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