Rtis Zee Biplane/artis Q/artis Q Zen(2017-08-25)

Recall Summary Artis Zee Biplane, Artis Q, and Artis Q Zen medical devices distributed across Canada are being recalled due to a device issue. This recall applies to devices distributed from 2017 onward and is classified as Class I, indicating a serious safety concern. The recall affects users of these medical imaging systems in Canada.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2017-09-26
Status
Closed
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/cba7c102-9229-4d3e-891e-cfa01dcc7206