Drug recall D-0540-2025
Product
BENLYSTA (belimumab) for injection, 400 mg/20 mL vial, Rx only, NDC 49401-102-01, GSK.
Reason for recall
CGMP Deviations; potential temperature excursions due to transit delays
Lots and codes
Lot: YK4W, Expiration date: 4/30/2029
Recall details
- Recalling firm
- Mckesson Medical-Surgical Inc. Corporate Office, Richmond, VA
- Quantity
- 3 Vials
- Distribution
- Within the U.S - OH, VA, FL.
- Type
- Voluntary: Firm initiated
- Recall initiated
- April 21, 2025
Related products
- Benlysta – drug information
- NDC 49401-102 Benlysta · Belimumab 400 mg/5mL · GlaxoSmithKline LLC
- NDC 49401-101 Benlysta · Belimumab 120 mg/1.5mL · GlaxoSmithKline LLC
- NDC 49401-088 Benlysta · Belimumab 200 mg/mL · GlaxoSmithKline LLC