Angiodynamics recalls NanoKnife 5-Probe Procedure Packs due to RFID programming errors that prevent probes from being recognized by the generator, causing procedure delays. Affected units include specific catalog and lot numbers.
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
Angi: The NanoKnife 5-Probe Procedure Pack 15 cm has been recalled because its RFID programming is faulty, causing the probes to not be recognized by the generator during surgery. This delay in procedure could impact surgical timing and patient care.
The faulty RFID programming prevents the NanoKnife probes from being recognized by the generator. This causes delays in the surgical procedure as the system cannot properly identify the probes during activation.
Surgical teams using the NanoKnife 5-Probe Procedure Pack 15 cm for soft tissue ablation are affected. Patients undergoing procedures with this specific pack may experience delays in surgery.
Check for catalog number 20400111, lot number 5762110, or UPN H787204001110 on the packaging. The product is sold under the brand Angiodynamics for surgical use.
Verify the catalog number 20400111, lot number 5762110, or UPN H787204001110 on the packaging to confirm if your unit is affected.
The NanoKnife 5-Probe Procedure Pack 15 cm has faulty RFID programming that prevents the probes from being recognized by the generator, causing delays in surgical procedures.
Check the product details for the catalog number 20400111, lot number 5762110, or UPN H787204001110 to confirm if your unit is affected. No specific remedy is provided in the recall notice.
The recall addresses a potential delay in surgical procedures due to the RFID programming issue, but no injury risk is mentioned in the official notice.
We’ve drafted a message you can send Angiodynamics to request your refund or repair — edit it as you like.
Subject: Recall Z-1381-2023 — Angiodynamics Angiodynamics Hello, I own a Angiodynamics that is covered by recall Z-1381-2023 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
