Class II · Moderate risk
Inflectra (infliximab-dyyb)
cGMP Deviations: Product intended for quarantine was inadvertently distributed.
Is Infliximab recalled?
Yes — there is an active recall. 1 ongoing FDA recall mention Infliximab (3 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 Infliximab. “Active” means an FDA recall is still ongoing; “closed” means it was terminated or completed. Checked against openFDA on Oct 10, 2026.
Infliximab recalls on record
none so far in 2026; 3 on record, newest first
Class II · Moderate risk
InFLIXimab 300 mg / 250 ml 0.9% NACL IVPB
Lack of Assurance of Sterility
Class II · Moderate risk
Remicade (Infliximab)
Lack of Assurance of Sterility
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