Mazor™ X System

Mazor X System Recall Summary The Mazor X System, a surgical robotic device used in spinal procedures, is being recalled across Canada due to a performance issue. This recall affects hospitals and surgical facilities that use this system. The FDA has classified this as a Class I recall, the most serious category.

Product
Mazor™ X System
Reason
Performance
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2025-12-19
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/e09aecaa-67ca-4d20-a8d5-80499a80e144