Public recall detail

Microdeep Depth Electrode

2025-08-08

medium
Recall Safety notice
Quick summary

Quick summary: Microdeep Depth Electrode. Date: 2025-08-08.

Recommended action

Recommended action: compare your product with the official notice and follow the instructions published by the official source.

Recall details

Quick summary: Microdeep Depth Electrode. Date: 2025-08-08.

Official details

Affected product details

Structured information extracted from the official recall notice. Confirm the identifiers and instructions in the original notice.

BrandDixi Medical
ProductMicrodeep Depth Electrode
IssueMedical devices - Performance
Recall classType I
IdentificationRA-77884

Affected products

ProductMicrodeep Depth Electrode
LotMore than 10 numbers, contact manufacturer.
ModelD08-05AM
Serial numberMore than 10 numbers, contact manufacturer.
DescriptionMicrodeep Depth Electrode
ProductMicrodeep Depth Electrode
LotMore than 10 numbers, contact manufacturer.
ModelD08-10AM
Serial numberMore than 10 numbers, contact manufacturer.
DescriptionMicrodeep Depth Electrode
ProductMicrodeep Depth Electrode
LotMore than 10 numbers, contact manufacturer.
ModelD08-15CM
Serial numberMore than 10 numbers, contact manufacturer.
DescriptionMicrodeep Depth Electrode
ProductMicrodeep Depth Electrode
LotMore than 10 numbers, contact manufacturer.
ModelD08-15AM
Serial numberMore than 10 numbers, contact manufacturer.
DescriptionMicrodeep Depth Electrode

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

What you should do

  • Retrieve and isolate the affected products.
Additional official information
AudienceHealthcare
CategoryHealth products - Medical devices - Neurology
CompaniesDixi Medical 2a Route De Pouligney Chaudefontaine, Marchaux-Chaudefontaine, France, 25640
Published byHealth Canada
Recall classType I
Alert / recall typeHealth product recall
Identification numberRA-77884
Background{}
CompaniesDixi Medical 2a Route De Pouligney Chaudefontaine, Marchaux-Chaudefontaine, France, 25640
AudiencesHealthcare
Source updated2025-08-11

Contains information licensed under the Open Government Licence – Canada. SafetyPulse is independent of the Government of Canada.

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