Glidescope Go (2021-07-07)
GlideScope Go Recall Summary The GlideScope Go medical device has been recalled across Canada due to a device malfunction. This recall affects healthcare facilities and providers who use this equipment. The FDA classified this as a Class I recall, indicating a serious issue with the device's function or safety.
- Reason
- Medical devices
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2021-07-22
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/d0b5c9b6-ac80-44de-a74e-8b6f837f6b40