Imris Hfd100 Head Fixation Device
IMRIS HFD100 Head Fixation Device Recall The IMRIS HFD100 Head Fixation Device is being recalled across Canada due to a performance issue. This device is used to stabilize a patient's head during medical procedures. The recall is classified as Class I, meaning there is a serious potential health risk.
- Product
- IMRIS HFD100 Head Fixation Device
- Reason
- Performance
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2025-12-17
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/ab687a10-280c-46d1-8d9f-60a660fcfd56