Xper Flex Cardio Physiomonitoring System-main Unit (2018-03-13)

Xper Flex Cardio Physiomonitoring System Recall The Xper Flex Cardio Physiomonitoring System main unit is being recalled across Canada. This is a Class I recall (the most serious type) affecting a medical device used for heart monitoring. The recall was issued on March 13, 2018, but no specific reason for the recall is provided in this notice.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2018-04-13
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/819f96f6-afcb-431b-af31-4e2d5b4260c6