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Tuftex® embolectomy and pruitt® occlusion catheters
Official notice
29 Apr 2025
Last checked
29 Apr 2025
An official Health Canada notice concerns Tuftex® embolectomy and pruitt® occlusion catheters. During internal product testing, we observed some packages to have incomplete seals (sterile barrier). If the sterile barrier of the packaged device is broken, there is a risk of contamination of the device and subsequent risk of infection if used. Recall start date: April 10, 2025 Published 2025-04-29.
What to do now
Contact the manufacturer if you require additional information.
Recall number
77348
Official notice
2025-04-29
The hazard
The hazard
During internal product testing, we observed some packages to have incomplete seals (sterile barrier). If the sterile barrier of the packaged device is broken, there is a risk of contamination of the device and subsequent risk of infection if used. Recall start date: April 10, 2025
How to check if you're affected
How to check if you're affected
Compare the product name and identifiers below with the item you own. Follow the official notice if they match.
Recall Numbers
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Affected products
Product 1
Product 2
Risk / hazard
Where it was sold
Where it was sold
The source does not list specific retailers. See the official notice for where affected products were sold.
Location 1
Affected area 1
Company & contacts
Company & contacts
Manufacturer
Phone
Brand: Lemaitre Vascular, Tuftex® Embolectomy And Pruitt® Occlusion Catheters.
Source & status
Source & status
Source
Tier
Category
Classification
App estimate
Recall details
Recall details
Recall number
Classification
Source tier
Documents, notices & source
See the official notice and source documents for full details.
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