O-arm O2 Imaging System (2019-11-15)

O-ARM O2 Imaging System Recall Summary The O-ARM O2 Imaging System has been recalled across Canada due to a medical device safety issue. This recall applies to all O-ARM O2 systems that were distributed in Canada. The recall is classified as Class I, which is the most serious type of recall classification.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2019-12-13
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/06e70f9f-1e9e-4258-8c3d-d9d07ac082e4