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
Reported: May 18, 2022 Initiated: May 2, 2022 #D-0855-2022
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
Reason for Recall
Defective container: loose crimp defect, potential loss of container integrity.
Details
- Recalling Firm
- Amgen, Inc.
- Units Affected
- 15,823
- Distribution
- Nationwide in the USA, Egypt and Lithuania.
- Location
- Thousand Oaks, CA
Frequently Asked Questions
What product was recalled? ▼
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. Recalled by Amgen, Inc.. Units affected: 15,823.
Why was this product recalled? ▼
Defective container: loose crimp defect, potential loss of container integrity.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on May 18, 2022. Severity: Moderate. Recall number: D-0855-2022.
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