Endopath Echelon Vascular Reloads

Endopath Echelon Vascular Reloads Recall Endopath Echelon Vascular Reloads devices are being recalled across Canada due to a performance issue. The devices may not function as intended during medical procedures. This is classified as a Class I recall, the most serious category.

Product
Endopath Echelon Vascular Reloads
Reason
Performance
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2025-05-02
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/9bb61fe5-aee9-4198-b01e-a483b342ec2d