Health product recall

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