Amgen, Inc. recalls MVASI (bevacizumab-awwb), Injection, For Intravenous Infusion After Dilution, 100 mg/4 ml, Single dose vial, Rx only, Manufactured by…
Defective container: loose crimp defect, potential loss of container integrity.
Read the official notice →- Date
- 2022-05-18
- Country
- United States
- Brand
- Amgen
- Product
- MVASI (bevacizumab-awwb), Injection, For Intravenous Infusion After Dilution, 100 mg/4 ml, Single dose vial, Rx only, Manufactured by…
- Classification
- Class II
- Units
- Nationwide in the USA, Egypt and Lithuania.
- Category
- Drugs & medical
- Source
- FDA · Drug
Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer
What to do
- Check the product name, strength and lot number against the official notice.
- Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
- Ask the pharmacy or supplier about a replacement or refund.
General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.
More Amgen recalls
- 2026-07-01
US- US
- 2025-03-26
- US
Amgen, Inc. recalls Neupogen (filgrastim) For Injection, 300mcg/1 mL, 1 mL Single Dose Vials, Rx Only, For Subcutaneous or Intravenous Use Only, Sterile…
Stability data does not support expiry: the products have the potential to be out of specification at the time of expiry of 36-months.
FDA · DrugAmgen, Inc.Nationwide in the U.S.A. and Belgium/Luxembourg, Brazil, Chile, Colombia,…Official notice →
Other drugs & medical recalls in the United States
- 2022-05-18
- US
Lula Holdings L.L.C. recalls Kill 'Dat Sanitizing Products Hand Sanitizer, 1 gallon (128 fl. oz.) 80% Alcohol, OTC, Manufactured by: Lula Holdings LLC, 15532 St.…
CGMP Deviations: FDA analysis found product to contain acetaldehyde above specification limits.
- US
SUN PHARMACEUTICAL INDUSTRIES INC recalls buPROPion Hydrochloride Extended-Release Tablet, USP (SR), 200 mg, 60-count bottle, Rx only Distributed by: Sun Pharmaceutical…
Presence Of Foreign Substance: Customer complaint for the presence of dark, gritty substance found within the bottle which was determined to be activated carbon from the desiccant canister inside the bottle.
- US
Fagron, Inc recalls SyrSpend SF Suspending Base, Cherry Flavored, packaged in a) 500mL bottles (NDC 51552-1123-5) and b) 4L bottles (NDC 51552-1123-9), Rx…
Microbial Contamination of Non-Sterile Product: Product is contaminated with Burkholderia gladioli.
- US
Viatris Inc recalls Xanax XR (alprazolam) extended-release tablets, 3 mg, 60-count bottle, Rx only, Distributed by Pharmacia & Upjohn Co, Division of Fizer…
Failed Dissolution Specifications: low out of specification results for dissolution.
- 2022-05-11
- US
Arthrex, Inc. recalls K-Wire, 1.35 mm x 170 mm
Products do not meet length and diameter specifications.
FDA · DeviceArthrex, Inc.Worldwide distribution - US Nationwide distribution in the states of OH, TN,…Official notice → - US
Olympus Corporation of the Americas recalls Ultrasonic Gastrovideoscope, GF-UC140P-AL5. Intended for endoscopic real-time ultrasound imaging.
GF-UC140P-AL5 is no longer a compatible endoscope for reprocessing in the OER-Pro and presents an infection control risk to patients