Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Propofol Injectable Emulsion Recalled by Hospira Inc. Due to Presence of Particulate Matter: Visible particles embedded in...
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
Propofol Injectable Emulsion, 1%, 200 mg/20 mL (10 mg/mL), 20 mL single patient infusion vial packaged in 5 Units x 20 mL per carton, Rx Only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-4699-30.
Quantity: 70,450 vials
Why Was This Recalled?
Presence of Particulate Matter: Visible particles embedded in the glass identified during a retain sample inspection.
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