Electrode Profonde
Brand(s)
Last updated
Summary
Product
Electrode Profonde
Issue
Medical devices - Manufacturing defect
What to do
Contact the manufacturer if you require additional information.
Affected products
| Affected Products | Lot or serial number | Model or catalog number |
|---|---|---|
| Electrode Profonde | All lots. | D08-08AT, D08-08AM, D08-15AT, D08-18ATM, D08-05AM, D08-05AT, D08-18CM, D08-12AT, D08-10AT, D08-12AM, D08-15BM, D08-18AT |
Issue
Detection of a deformation in the blister pack of the primary packaging during a production control which could lead to a perforation. Secondary packaging is not affected.
Recall start date: Nov 19, 2021
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
General public
Health professionals
Hospitals
Recall class
Type II
Identification number
RA-63753
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