Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
0.5% Bupivacaine HCl and Epinephrine 1:200 Recalled by Hospira Inc. Due to Lack of Assurance of Sterility; potential for vial...
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
0.5% Bupivacaine HCl and Epinephrine 1:200,000 Inj., 10 mL, Single-Dose Vial, NDC 0409-9045-01, Hospira, Inc., Lake Forest, IL 60045
Quantity: 187,150 vials
Why Was This Recalled?
Lack of Assurance of Sterility; potential for vial breakage
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