Cerebase Da Guide Sheath
Brand(s)
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 |
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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