BENLYSTA (belimumab) for injection, 400 mg/20 mL vial, Rx only, NDC 49401-102-01, GSK.
Reported: July 30, 2025 Initiated: April 21, 2025 #D-0540-2025
Product Description
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
Details
- Recalling Firm
- Mckesson Medical-Surgical Inc. Corporate Office
- Units Affected
- 3 Vials
- Distribution
- Within the U.S - OH, VA, FL.
- Location
- Richmond, VA
Frequently Asked Questions
What product was recalled? ▼
BENLYSTA (belimumab) for injection, 400 mg/20 mL vial, Rx only, NDC 49401-102-01, GSK.. Recalled by Mckesson Medical-Surgical Inc. Corporate Office. Units affected: 3 Vials.
Why was this product recalled? ▼
CGMP Deviations; potential temperature excursions due to transit delays
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on July 30, 2025. Severity: Moderate. Recall number: D-0540-2025.
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