Xper Flex Cardio Physiomonitoring System-main Uni

Xper Flex Cardio Physiomonitoring System Recall The Xper Flex Cardio Physiomonitoring System main unit is being recalled across Canada. The recall was issued due to a medical device safety concern. This recall affects users of this cardiomonitoring device in Canada.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2017-09-11

Status

Closed

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/6701c06b-210f-43b1-a55e-7fc6849712b7