Xper Flex Cardio Physiomonitoring System-main Unit (2018-11-18)

Recall Summary The Xper Flex Cardio Physiomonitoring System main unit is being recalled across Canada due to a medical device issue. This device was distributed nationwide and has been classified as a Class I recall, indicating a serious safety concern. The recall affects all users of this physiomonitoring system in Canada.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2018-11-30

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/02a8b027-6ab5-4c49-98f6-537cb71d42bd