Xper Flex Cardio Physiomonitoring System (2021-04-01)

XPER FLEX CARDIO PHYSIOMONITORING SYSTEM Recall The XPER FLEX CARDIO PHYSIOMONITORING SYSTEM is being recalled in Canada because it is a medical device that does not meet regulatory requirements. This recall affects all units of this device that were distributed across Canada. The device is used for heart monitoring and physiological measurements.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2021-04-14

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/9b0c8080-b950-464b-9b01-1e45db3043c6