Recall Record

Ventura, CA, United States

Neurovision Medical Products Inc recalls

3 recalls recorded since 2018, most recently on 19 May 2025. 2 are listed as ongoing. Status and classification are as published by the FDA.

Recalls3
Ongoing (FDA)2
Terminated or completed1
Class I (FDA)0

Ongoing Class II Medical devices

Recall started
19 May 2025
Reason
Product packaging contains the wrong part number and kit contents.
Distribution
US distribution to CA only
Initiated
Voluntary: Firm initiated
Recall number
Z-2100-2025

Ongoing Class II Medical devices

Recall started
1 July 2024
Reason
mislabeling; EMG RLN monitoring kit labeling contains the incorrect tube size.
Distribution
US Nationwide distribution.
Initiated
Voluntary: Firm initiated
Recall number
Z-2719-2024

Terminated Class II Medical devices

Recall started
21 July 2020
Terminated
30 April 2021
Reason
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.
Distribution
Worldwide distribution - US Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, CT, FL, GA, HI, IL, IN, KS, MA, MD, MI, MN, MO, MS, NE, NY, OH, OR, PA, SC, SD, TN, TX, WA, WI and the countries of Canada, Dominican Republic, Hong Kong.
Initiated
Voluntary: Firm initiated
Recall numbers
Z-2902-2020, Z-2907-2020, Z-2903-2020, Z-2904-2020, Z-2900-2020, Z-2905-2020, Z-2906-2020, Z-2901-2020, Z-2908-2020

A terminated FDA recall means the FDA has determined that all reasonable efforts to remove or correct the product have been made. What statuses mean.