Neurovision recalls Cobra x5 EMG tubes with softening insulation that may stop signal transmission. Affected units have specific lot numbers. Stop using if you have the product.
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 EMG monitoring tubes that may have softened insulation, which could cause signal loss during nerve monitoring. This affects medical professionals using the tubes in surgeries. If you have the product, stop using it immediately.
The electrode insulation softens over time, making it prone to damage from scratching or bending. This can stop the EMG signal from reaching the monitor, rendering the tube unusable during critical nerve monitoring procedures.
Medical professionals who use the Cobra x5 EMG tubes for nerve monitoring during surgery are most at risk. Patients undergoing procedures with this device could be affected if the tube fails.
Check for the model 'Cobra x5 1-Ch EMG ET Tube, 7.0mm, REF LTE700M-5' with lot numbers listed in the recall notice. The product is sterile and used for continuous nerve monitoring during surgery.
Immediately stop using the Cobra x5 EMG tube if you have it, as it may cause signal loss during nerve monitoring.
The electrode insulation may soften over time, causing damage that stops signal transmission during nerve monitoring.
The tube may not transmit EMG signals to the monitor, which could affect nerve monitoring during surgery.
Look for the model 'Cobra x5 1-Ch EMG ET Tube, 7.0mm, REF LTE700M-5' with specific lot numbers listed in the recall notice.
We’ve drafted a message you can send Neurovision to request your refund or repair — edit it as you like.
Subject: Recall Z-2904-2020 — Neurovision Neurovision Hello, I own a Neurovision that is covered by recall Z-2904-2020 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.
