Neurovision Medical Products Inc: Device Recall
Recall #Z-2719-2024 · 07/01/2024
Class II: Risk
Recall Details
- Recall Number
- Z-2719-2024
- Classification
- Class II
- Product Type
- Device
- Recalling Firm
- Neurovision Medical Products Inc
- Status
- Ongoing
- Date Initiated
- 07/01/2024
- Location
- Ventura, CA, United States
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 5 BOXES (25 single kits)
Reason for Recall
mislabeling; EMG RLN monitoring kit labeling contains the incorrect tube size.
Product Description
Cobra, 3-Plate EMG ET Tube, 6.0mm, REF: LTE7003PM, not made with natural rubber latex, Rx Only, STERILEEO
Distribution Pattern
US Nationwide distribution.
Other Recalls by Neurovision Medical Products Inc
- Class II: Risk 05/19/2025
Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.