Xper Flex Cardio Physiomonitoring System-main Unit (2017-11-17)

Recall Summary The XPER FLEX CARDIO PHYSIOMONITORING SYSTEM-MAIN UNIT is being recalled across Canada due to a medical device issue classified as Class I, the most serious type. This device was distributed nationwide and is used for heart monitoring and physiological measurements. The recall affects all users who have this main unit in their possession.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2017-12-08

Status

Closed

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/da71c875-d1e9-406b-8498-5765188ce84a