Official recall record
Microdeep Depth Electrode
- Issuing authority
- Health Canada — Medical Devices
- Published
- 2025-08-08
- Last updated (per notice)
- 2025-08-11
- Country of alert
- Canada
- Alert level
- Type I
- Alert type
- recall
What the authority reported
A manufacturing defect has been identified in the caps used in certain Dixi Medical devices. Although the cap is screwed onto the guiding screw, it is possible for the electrodes to slip inside. this indicates that the clamping function provided by the screw may not be fully effective, potentially compromising the safe positioning of the device. Customers are requested to isolate the affected devices. Recall start date: July 30, 2025
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.
ProductGuru Recalls republishes official safety information with attribution. We are not
the issuing authority and this page is not advice. If this product is a medical device or
medication, speak to a doctor or pharmacist. Found an error?
Report it — corrections are published.