Serious health hazard — there is a reasonable probability that use of or exposure to this product will cause serious adverse health consequences or death.
0.25% Bupivacaine HCl Injection Recalled by Hospira Inc. Due to Presence of particulate matter: visible free floating and...
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
0.25% Bupivacaine HCl Injection, USP, 2.5 mg/mL, 30 mL, Single-dose, Hospira Inc., Lake Forest, IL 60045, NDC 0409-1159-02
Quantity: 118,100 vials
Why Was This Recalled?
Presence of particulate matter: visible free floating and partially embedded particulate matter in the glass vials.
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