Amgen, Inc. recalls MVASI (bevacizumab-awwb), Injection, For Intravenous Infusio
See all recalls from Amgen, Inc. →Recalled 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
Hazard / Issue
Defective container: loose crimp defect, potential loss of container integrity.
Issued by
FDA
Distribution: Nationwide (United States)
Lot/Code Info: Lots: 1142258, 1143196, Exp. 09/24
✅ 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 MVASI (bevacizumab-awwb), Injection, For →If you were harmed by this recalled product, Top Class Actions lists active class action lawsuits and settlements that may apply to you.
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