Class II Recall

Amgen, Inc.

Product
MVASI (bevacizumab-awwb), Injection, For Intravenous Infusion After Dilution, 100 mg/4 ml, Single dose vial, Rx only, Manufactured by Amgen Inc. Thousand Oaks, CA 91320-1799, NDC 55513-0206-01
Reason
Defective container: loose crimp defect, potential loss of container integrity.
Classification
Class II
Status
Terminated
Lot
Lots: 1142258, 1143196, Exp. 09/24
Date
Disclaimer: This tool indexes published US FDA drug-enforcement recall records from all countries, limited to the latest five years. A company or product not appearing here is not proof that it is compliant, approved, safe, or free of FDA action.
Amgen, Inc. — Class II Recall | MedicineWatch US