Glidescope Gotm Video Laryngoscopy System (2019-03-14)
GlideScope Go Video Laryngoscopy System Recall The GlideScope Go video laryngoscopy system is being recalled across Canada. The device is used by medical professionals to help visualize the airway during intubation procedures. This is a Class I recall, which is the most serious classification, indicating the device could cause serious injury or death.
- Reason
- Medical devices
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2019-03-28
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/617514a0-2792-43d9-aa54-b39ad26436fe