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All product recalls associated with Neurovision Medical Products Inc.
Total Recalls
9
Past Year
1
Class I (Serious)
0
Most Recent
May 2025
Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.
Product packaging contains the wrong part number and kit contents.
mislabeling; EMG RLN monitoring kit labeling contains the incorrect tube size.
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.