Product Wiki · Recalls · Health Canada — Medical Devices

ENVEO PRO DELIVERY CATHETER SYSTEM (2021-06-09) — recall 62560

Health Canada — Medical Devices · Canada · 2021-06-30 · Type II

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Agency
Health Canada — Medical Devices
Recall identifier
62560
Date of alert
2021-06-30
Country / jurisdiction
Canada
Risk level
Type II
Risk type
recall
Product category
Medical devices
Product type
Medical devices
Reported risk: Medtronic is voluntarily recalling EnVeoR Pro Delivery Catheters with a manufacturing date before 11-Jul-2020. Medtronic is taking this action to reduce the potential for actuator separation within the subset. Actuator separation may occur during valve loading on the delivery system, advancement, deployment or recapture of the valve. Through March 2021, the reported rate of actuator separation on the original design version was 0.18% out of 270,071 sold worldwide. If the actuator separates during a procedure, it could lead to procedure delays, hypotension, secondary procedure, or tissue damage. The actuator is an external component of the handle of the Enveo Pro Delivery Catheters.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/enveo-pro-delivery-catheter-sy

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