Medtronic Xomed recalls specific models of NIM TriVantage EMG Endotracheal Tubes (6.0MM ID, 7.0MM ID, 8.0MM ID) due to reported noise, lead-off or high impedance issues, and intermittent nerve monitoring problems.
Firm received reports of customers experiencing noise from the NIM System, lead-off or high impedance issues, or loss of/intermittent nerve monitoring,
Medtronic Xomed is recalling specific models of NIM TriVantage EMG Endotracheal Tubes that have been reported to cause noise, lead-off or high impedance issues, and intermittent nerve monitoring problems. These tubes are used in medical settings for monitoring nerve function during procedures.
The recalled tubes have been reported to cause noise, lead-off or high impedance issues, and intermittent nerve monitoring problems. These issues can affect the accuracy of nerve monitoring during medical procedures, potentially leading to incorrect treatment decisions.
Healthcare professionals and medical facilities that use the recalled NIM TriVantage EMG Endotracheal Tubes for nerve monitoring procedures are most at risk. Patients using these tubes during medical procedures may experience monitoring issues.
Check for the model numbers 8229706 (6.0MM ID), 8229707 (7.0MM ID), or 8229708 (8.0MM ID) on the tube packaging or labels. Also look for the specific serial numbers and GTINs listed in the recall notice.
Verify the model number and serial numbers against the list provided in the recall notice to confirm if your tubes are affected.
The recall indicates reported issues with noise, lead-off or high impedance, and intermittent nerve monitoring, but the tubes are not considered unsafe for use in normal medical procedures.
Check the model numbers (8229706, 8229707, 8229708) and serial numbers listed in the recall notice to see if your tubes match.
The recall does not require stopping use; healthcare providers should check the model and serial numbers to ensure they are not affected.
We’ve drafted a message you can send Medtronic Xomed to request your refund or repair — edit it as you like.
Subject: Recall Z-0696-2024 — Medtronic Xomed Medtronic Xomed Hello, I own a Medtronic Xomed that is covered by recall Z-0696-2024 from Medtronic Xomed. 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.
