FDAApril 24, 2020device

AngioDynamics NanoKnife Disposable Single Electrode Probes, Irreversible Electroporation (IRE) Device, 15 cm IRE Single Electrode RFID Activation, PG. Catalog No. 20400103

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Programming issue affected RFID function of a single lot and did not allow the NanoKnife probes to be recognized by the NanoKnife generator.

What to do

FDA enforcement status: Terminated

Brands named

angiodynamics

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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