Cyberknife® Treatment Delivery System

CyberKnife® Treatment Delivery System Recall The CyberKnife® Treatment Delivery System, a medical device used to deliver radiation therapy, is being recalled across Canada due to a device performance issue. This is classified as a Class II recall, meaning the issue could cause adverse health effects but is not life-threatening. The recall affects patients and healthcare facilities in Canada that use this radiation therapy system.

Product
CyberKnife® Treatment Delivery System
Reason
Device performance issue
Classification
Class II
Category
medical device recall
Country
Canada
Agency
HC-DEVICES
Recall date
2026-06-22
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/281c6079-e2df-4327-8fa1-58df506ba8c2