Microdeep Depth Electrode
Brand(s)
Last updated
Summary
Product
Microdeep Depth Electrode
Issue
Medical devices - Performance
What to do
Retrieve and isolate the affected products.
Audience
Healthcare
Affected products
| Affected products | Lot or serial number | Model or catalogue number |
|---|---|---|
| Microdeep Depth Electrode | More than 10 numbers, contact manufacturer. | D08-05AM |
| Microdeep Depth Electrode | More than 10 numbers, contact manufacturer. | D08-10AM |
| Microdeep Depth Electrode | More than 10 numbers, contact manufacturer. | D08-15CM |
| Microdeep Depth Electrode | More than 10 numbers, contact manufacturer. | D08-15AM |
Issue
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
Additional information
Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - Neurology
Companies
| Dixi Medical |
| 2a Route De Pouligney Chaudefontaine, Marchaux-Chaudefontaine, France, 25640 |
Published by
Health Canada
Audience
Healthcare
Recall class
Type I
Identification number
RA-77884
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