FDAMarch 2, 2023device

NanoKnife 5-Probe Procedure Pack 15 cm - Activation. Indicated for the surgical ablation of soft tissue. Catalog Number: 20400111 UPN: H787204001110

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

The hazard

Not programmed in accordance with specification. The programming affects the RFID function and does not allow the NanoKnife probes to be recognized by the NanoKnife generator resulting in a delay in procedure

What to do

FDA enforcement status: Ongoing

Brands named

angiodynamics

UPCs

15051684029643

Recall history

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

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