Glidescope Core System (2019-08-28)
GlideScope Core System Recall Summary The GlideScope Core System is being recalled in Canada due to a medical device issue. This recall affects GlideScope Core Systems distributed across Canada. The FDA has classified this as a Class I recall, which is the most serious classification.
- Reason
- Medical devices
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2019-09-20
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/a894407c-c54c-4e78-99db-7f15291ad85e