Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
BENLYSTA (belimumab) for injection Recalled by Mckesson Medical-Surgical Inc. Corporate Office Due to CGMP Deviations; potential temperature excursions due to transit...
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 Mckesson Medical-Surgical Inc. Corporate Office directly.
Affected Products
BENLYSTA (belimumab) for injection, 400 mg/20 mL vial, Rx only, NDC 49401-102-01, GSK.
Quantity: 3 Vials
Why Was This Recalled?
CGMP Deviations; potential temperature excursions due to transit delays
Where Was This Sold?
This product was distributed to 3 states: FL, OH, VA
About Mckesson Medical-Surgical Inc. Corporate Office
Mckesson Medical-Surgical Inc. Corporate Office has 276 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report