Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
NanoKnife 5-Probe Procedure Pack 15 cm - Activation. Indicated for Recalled by Angiodynamics, Inc. Due to Not programmed in accordance with specification. The programming...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Angiodynamics, Inc. directly.
Affected Products
NanoKnife 5-Probe Procedure Pack 15 cm - Activation. Indicated for the surgical ablation of soft tissue. Catalog Number: 20400111 UPN: H787204001110
Quantity: 10 boxes( 5 probes/box)
Why Was This Recalled?
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
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Angiodynamics, Inc.
Angiodynamics, Inc. has 74 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report