Nerveana Cn X/rln Monitoring Kit With 1-channel Cobra Emg Et Tube, Cobra 1 & 2-channel Emg Et Tube And 2 Subdermal Needles (2020-07-22)
Recall Summary Nerveana CN X/RLN monitoring kits and related EMG equipment have been recalled across Canada. The recall involves 1-channel and 2-channel Cobra EMG ET tube devices, along with subdermal needle components. This is classified as a Class I recall, meaning there is a serious potential health risk associated with these medical devices.
- Reason
- Medical devices
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2020-08-14
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/ad79543d-88e3-4612-b4d6-d349a21804b7