Medical DeviceJul 16, 2025
Hummingbird Stimulated EMG Kit with Hummingbird recall — FDA Z-2100-2025
Product packaging contains the wrong part number and kit contents.
Class IIFDA: OngoingNeurovision Medical Products Inc.
Recall history in this database
Classification mix: Class II: 11.
Medical DeviceSep 4, 2024
Neurovision Medical Products Cobra, 3-Plate EMG ET Tube, 6.0mm, REF: LTE7003PM, not made recall — FDA Z-2719-2024
mislabeling; EMG RLN monitoring kit labeling contains the incorrect tube size.
Class IIFDA: OngoingNeurovision Medical Products Inc.
Medical DeviceSep 2, 2020
Neurovision Medical Products Nerveana x5 RLN Monitoring Kit with Cobra 1-Ch EMG ET Tube, 8.0 recall — FDA Z-2902-2020
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,…
Class IIFDA: TerminatedNeurovision Medical Products Inc.
Medical DeviceSep 2, 2020
Neurovision Medical Products Cobra x5 2-Ch EMG ET Tube, 7.0mm, REF: LTE700DCM-5, Rx Only recall — FDA Z-2907-2020
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,…
Class IIFDA: TerminatedNeurovision Medical Products Inc.
Medical DeviceSep 2, 2020
Neurovision Medical Products Cobra x5 1-CH EMG ET Tube, 6.0mm, REF: LTE700S-5, Rx Only recall — FDA Z-2903-2020
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,…
Class IIFDA: TerminatedNeurovision Medical Products Inc.
Medical DeviceSep 2, 2020
Neurovision Medical Products Cobra x5 1-Ch EMG ET Tube, 7.0mm, REF LTE700M-5, Rx Only recall — FDA Z-2904-2020
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,…
Class IIFDA: TerminatedNeurovision Medical Products Inc.
Medical DeviceSep 2, 2020
Neurovision Medical Products Nerveana x5 RLN Monitoring Kit with Cobra 1-Ch EMG ET Tube recall — FDA Z-2900-2020
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,…
Class IIFDA: TerminatedNeurovision Medical Products Inc.
Medical DeviceSep 2, 2020
Neurovision Medical Products Cobra x5 1-Ch EMG ET Tube, 8.0mm, REF: LTE700L-5, Rx Only recall — FDA Z-2905-2020
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,…
Class IIFDA: TerminatedNeurovision Medical Products Inc.
Medical DeviceSep 2, 2020
Neurovision Medical Products Cobra x5 2-Ch EMG ET Tube, 6.0mm, REF: LTE700DCS-5, Rx Only recall — FDA Z-2906-2020
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,…
Class IIFDA: TerminatedNeurovision Medical Products Inc.
Medical DeviceSep 2, 2020
Neurovision Medical Products Nerveana x5 RLN Monitoring Kit with Cobra 1-Ch EMT ET Tube recall — FDA Z-2901-2020
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,…
Class IIFDA: TerminatedNeurovision Medical Products Inc.
Medical DeviceSep 2, 2020
Neurovision Medical Products Cobra x5 2-Ch EMG ET Tube, 8.0mm, REF: LTE700DCL-5, Rx Only recall — FDA Z-2908-2020
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,…
Class IIFDA: TerminatedNeurovision Medical Products Inc.
Understanding this recall history
This page summarizes recall records in which the official source identifies Neurovision Medical Products Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.