Angiodynamics recalls 15 cm IRE Single Electrode Probes due to RFID programming issue preventing recognition by the generator. Affected units may not function properly during medical procedures.
Programming issue affected RFID function of a single lot and did not allow the NanoKnife probes to be recognized by the NanoKnife generator.
Angiodynamics is recalling 15 cm IRE Single Electro: Probes because a programming issue prevents the probes from being recognized by the NanoKnife generator. This could lead to improper use during medical procedures if the probes aren't detected by the device.
The RFID programming issue means the probes cannot be detected by the NanoKnife generator during use. This could result in the procedure not functioning correctly if the probes aren't recognized by the device.
Medical professionals using the AngioDynamics NanoKnife system for irreversible electroporation procedures are most likely affected. Patients receiving these procedures may also be impacted if the probes aren't properly recognized.
Check for the product name 'AngioDynamics NanoKnife Disposable Single Electrode Probes, 15 cm IRE Single' with catalog number 20400103 and lot number 5577754.
Verify the catalog number (20400103) and lot number (5577754) on the probe packaging.
The recall is due to a programming issue that affects the RFID function of the probes, preventing them from being recognized by the NanoKnife generator.
The official recall notice does not specify a remedy, so contact Angiodynamics directly for guidance.
The recall indicates a potential issue with device recognition during medical procedures, but no specific injury risk is mentioned.
We’ve drafted a message you can send Angiodynamics to request your refund or repair — edit it as you like.
Subject: Recall Z-0073-2022 — Angiodynamics Angiodynamics Hello, I own a Angiodynamics that is covered by recall Z-0073-2022 from Angiodynamics. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
