FDAMay 2, 2022drug

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

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Defective container: loose crimp defect, potential loss of container integrity.

What to do

FDA enforcement status: Terminated

Brands named

amgen

UPCs

55513020601

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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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 — Recall Details · AllClear