FDA recall record

Amgen MVASI (bevacizumab-awwb), Injection, For Intravenous Infusion After Dilution, 100 mg/4 recall — FDA D-0855-2022

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

Class IIclassification
D-0855-2022official record ID
May 18, 2022report date

Recall record at a glance

Official recordD-0855-2022
CategoryDrug Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmAmgen, Inc.
Report dateMay 18, 2022
Recall initiation dateMay 2, 2022
Quantity15,823
LocationThousand Oaks, CA, United States

Official product description

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

Why the product was recalled

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

Distribution information

Nationwide in the USA, Egypt and Lithuania.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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