Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Labetalol Hydrochloride Injection Recalled by Hospira Inc. Due to Presence of Particulate Matter; metal embedded in the...
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
Labetalol Hydrochloride Injection, USP, 100 mg/20 mL (5 mg/mL), 20 mL Multidose Vial, packaged 50/20 mL glass vials/carton, Hospira, Inc., Lake Forest, IL 60045 --- NDC 0409-2267-20
Quantity: 45,448 vials
Why Was This Recalled?
Presence of Particulate Matter; metal embedded in the glass vial and visible particles floating in the solution
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