Optima Xr220amx X-ray System

Summary GE Healthcare is recalling the Optima XR220amx X-Ray System across Canada due to a performance issue. This recall affects medical facilities that use this X-ray equipment. The FDA classified this as a Class I recall, which indicates a serious issue with the device's function.

Product
Optima XR220amx X-Ray System
Reason
Performance
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2024-12-18
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/e71d3f86-c972-48c8-bf88-cf7256bcc540