Health product recall

Cerebase Da Guide Sheath

Last updated

Summary

Product
Cerebase Da Guide Sheath
Issue
Medical devices - Performance issue
What to do

Contact the manufacturer if you require additional information. 

Audience
Healthcare

Affected products

Affected products Lot or serial number Model or catalogue number
Cerebase Da Guide Sheath More than 10 numbers, contact manufacturer. GS9080SD GS9095SD GS9090SD

Issue

Medos has received an increase in complaints for Cerebase Da Guide Sheath with reports of fractures at the distal end, which may result in surgical procedural delay, vascular injury and in extreme rare occasions it may result in embolism.

Recall start date: February 7, 2024

Additional information

Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - Cardiovascular
Companies
Medos International Sarl
Chemin-Blanc 38, Le Locle, Switzerland, 2400
Published by
Health Canada
Audience
Healthcare
Recall class
Type II
Identification number
RA-75080

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