Official recall record
Cerebase Da Guide Sheath
- Issuing authority
- Health Canada — Medical Devices
- Published
- 2024-02-16
- Country of alert
- Canada
- Alert level
- Type II
- Alert type
- recall
What the authority reported
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
What to do
Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.
Verify at the source:
Health Canada — Medical Devices — official record →
Record last checked against the registry on 2026-05-31.
Record last checked against the registry on 2026-05-31.
ProductGuru Recalls republishes official safety information with attribution. We are not
the issuing authority and this page is not advice. If this product is a medical device or
medication, speak to a doctor or pharmacist. Found an error?
Report it — corrections are published.