Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
5% Lidocaine HCl and 7.5% Dextrose Injection Recalled by Hospira Inc. Due to Presence of Particulate Matter; report of visible particulates...
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
5% Lidocaine HCl and 7.5% Dextrose Injection, USP, 2 mL Single Dose Ampuls, Rx only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-4712-01
Quantity: 86,400 ampuls
Why Was This Recalled?
Presence of Particulate Matter; report of visible particulates in the glass ampule
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