Mckesson Medical-Surgical Inc. Corporate Office recalls BENLYSTA (belimumab) for injection, 400 mg/20 mL vial, Rx o
See all recalls from Mckesson Medical-Surgical Inc. Corporate Office →Recalled Product
BENLYSTA (belimumab) for injection, 400 mg/20 mL vial, Rx only, NDC 49401-102-01, GSK.
Hazard / Issue
CGMP Deviations; potential temperature excursions due to transit delays
Issued by
FDA
Affected States: OH, VA, FL
Lot/Code Info: Lot: YK4W, Expiration date: 4/30/2029
✅ What Should You Do?
- 1Stop taking this medication and contact your doctor or pharmacist immediately.
- 2Do NOT flush medications down the drain — use an FDA-approved drug take-back program.
- 3Check the lot number on your bottle or packaging against the recalled lots listed above.
- 4Report adverse events to FDA MedWatch or call 1-800-FDA-1088.
Looking for a safe alternative?
Search Amazon for BENLYSTA (belimumab) for →If you were harmed by this recalled product, Top Class Actions lists active class action lawsuits and settlements that may apply to you.
Get the next US recall alert before it hits the news.
Free. Weekly digest or instant alerts. Unsubscribe anytime.
CAN-SPAM compliant · No spam · Unsubscribe anytime