Class II · Moderate risk
Bortezomib for Injection 3.5mg/Vial
Lack of Sterility Assurance
Is Bortezomib recalled?
Yes — there is an active recall. 1 ongoing FDA recall mention Bortezomib (4 total). Check the affected lots below.
Most common reason: Sterility / contamination (2 of these recalls)
Recalls are matched by product description. A recall usually affects specific lots, not every package of Bortezomib. “Active” means an FDA recall is still ongoing; “closed” means it was terminated or completed. Checked against openFDA on Oct 10, 2026.
Bortezomib recalls in 2026
1 initiated in 2026, 4 in total — newest first
Class III · Low risk
Bortezomib
Failed stability specifications
Class II · Moderate risk
BORTEZOMIB 2.5 mg / 1 ML SQ SYRINGE
Lack of Assurance of Sterility
Class II · Moderate risk
VELCADE (bortezomib)
Defective Container: Confirmed reports of loose vial crimps.
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