Cyberknife M6 Fim System

CyberKnife M6 FIM System Recall The CyberKnife M6 FIM System, a radiation therapy device used to treat tumors and other conditions, is being recalled across Canada due to a software issue that could cause the device to operate unexpectedly. The problem affects all CyberKnife M6 FIM Systems that have been distributed in Canada. This is a Class I recall, which is the most serious type.

Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2017-02-09
Status
Closed
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/f01c062f-2343-4bc1-b681-7962b1020fb8