Neurovision recalls Nerveana x5 RLN Monitoring Kit with Cobra EMG tube due to risk of signal loss from electrode insulation softening over time. Affected kits include specific lot numbers.
The electrode insulating material on the Cobra EMG ET tube used for continuous EMG monitoring may soften over time so that it may be more susceptible to damage by scratching or bending, which could stop or inhibit the EMG signal transmission of the electrodes to the monitor and render the device not usable.
Neurovision is recalling its Nerveana x5 RLN Monitoring Kit with Cobra 1-Ch EMG ET tube because the electrode insulation may soften, causing signal transmission issues. This could lead to the device becoming unusable during critical medical procedures.
The electrode insulating material on the Cobra EMG tube can soften over time, making it more prone to damage from scratching or bending. This damage may stop or inhibit the EMG signal transmission to the monitor, rendering the device unusable during critical medical procedures.
Healthcare professionals using the Nerveana x5 RLN Monitoring Kit for continuous EMG monitoring during surgery are most at risk. Patients undergoing procedures requiring nerve monitoring may be affected if the kit is used.
Check for the product name 'Nerveana x5 RLN Monitoring Kit with Cobra 1-Ch EMG ET Tube, 8.0 mm' and the reference number NVTKIT-C8-5. The kit was sold with specific lot numbers listed in the recall notice.
Look for the lot number on the kit packaging, which is one of the listed numbers such as 012320C or 120219G.
Reach out to Neurovision Medical Products Inc for guidance on next steps if you have the recalled kit.
The electrode insulating material on the Cobra EMG tube may soften over time, causing it to be more susceptible to damage that could stop signal transmission to the monitor.
Damage could stop or inhibit the EMG signal transmission, rendering the device unusable during critical medical procedures.
Check for the product name 'Nerveana x5 RLN Monitoring Kit with Cobra 1-Ch EMG ET Tube, 8.0 mm' and reference number NVTKIT-C8-5 with one of the listed lot numbers.
We’ve drafted a message you can send Neurovision to request your refund or repair — edit it as you like.
Subject: Recall Z-2902-2020 — Neurovision Neurovision Hello, I own a Neurovision that is covered by recall Z-2902-2020 from Neurovision. 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.
