Lasertubus Endotracheal Tube (2020-06-01)
Lasertubus Endotracheal Tube Recall The Lasertubus Endotracheal Tube, a medical device used in airway management, has been recalled across Canada. The recall is classified as Class I, indicating a serious safety concern. This recall affects all Lasertubus Endotracheal Tubes distributed in Canada.
- Reason
- Medical devices
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2020-06-16
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/62e07174-3f38-4810-a83e-5d4ba305c615