Published recall report · Quality failureUpdated · 1 yr 2 mo ago
Mckesson Medical-Surgical Inc. Corporate Office recall: BENLYSTA (belimumab) for injection, 400 mg/20 mL vial, Rx only, NDC 49401-102-01, GSK.
BENLYSTA (belimumab) for injection, 400 mg/20 mL vial, Rx only, NDC 49401-102-01, GSK.
Current recall status is unverified. FDA does not update drug-enforcement status after publication. Check the latest official information or ask a pharmacist.
What to do
Check the lot number on your pack against this recall and follow the firm's instructions. Do not stop taking a prescribed medicine without talking to a pharmacist or doctor first.
FDA public enforcement report, opens in a new tabWhich products
BENLYSTA (belimumab) for injection, 400 mg/20 mL vial, Rx only, NDC 49401-102-01, GSK.
- Producer
- Mckesson Medical-Surgical Inc. Corporate Office
- Brand
- BENLYSTA
YK4W
- Dates on pack
- Lot: YK4W, Expiration date: 4/30/2029
More detail
CGMP Deviations; potential temperature excursions due to transit delays
In the news
Reporting from news publishers. Follow the official notice for product advice.
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