Class II · Moderate risk Ongoing
Bortezomib for Injection 3.5mg/Vial, 10 mL per Single-Dose Vial, For Intravenous or Subcutaneous Use, Manufactured for: Somerset…
Reason Lack of Sterility Assurance
4 FDA recalls mention Bortezomib. The most recent are listed below.
Recalls are matched by product description. A recall usually affects specific lots, not every package of Bortezomib.
Reason Lack of Sterility Assurance
Reason Failed stability specifications
Reason Lack of Assurance of Sterility
Reason Defective Container: Confirmed reports of loose vial crimps.
Tell us which medications you take. If the FDA recalls one, we email you - in plain English, with what to do. Free.