Official recall record
IMRIS HFD100 Head Fixation Device
- Issuing authority
- Health Canada — Medical Devices
- Published
- 2025-12-17
- Country of alert
- Canada
- Alert level
- Type II
- Alert type
- recall
What the authority reported
IMRIS is conducting a voluntary recall to address a potential safety risk associated with use of the HFD100 Head Fixation Device and will be completing corrective action to remove and replace the torque screw component in all HFD100 Head Fixation Devices at all affected customer sites.
What to do
Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.
Verify at the source:
Health Canada — Medical Devices — official record →
Record last checked against the registry on 2026-05-31.
Record last checked against the registry on 2026-05-31.
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