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Ivascular navitian
Official notice
24 Mar 2026
Last checked
24 Mar 2026
An official Health Canada notice concerns Ivascular navitian. A potential risk has been identified through post-market surveillance: deterioration of the outer layer of the thinner distal segment of the device, which could lead to the loss of material fragments when used in extremely calcified lesions. Published 2026-03-24.
What to do now
Contact the manufacturer if you require additional information.
Recall number
81788
Official notice
2026-03-24
The hazard
The hazard
A potential risk has been identified through post-market surveillance: deterioration of the outer layer of the thinner distal segment of the device, which could lead to the loss of material fragments when used in extremely calcified lesions.
How to check if you're affected
How to check if you're affected
Compare the VIN on your vehicle against the official list. If your VIN is listed, follow the official notice.
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Where it was sold
Where it was sold
The source does not list specific retailers. See the official notice for where affected vehicles were sold.
Location 1
Affected area 1
Company & contacts
Company & contacts
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Brand: Life Vascular Devices Biotech S.l.
Source & status
Source & status
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Recall details
Recall details
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Documents, notices & source
See the official notice and source documents for full details.
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