Xper Flex Cardio Physiomonitoring System - Main Unit (2017-11-14)

Recall Summary The XPER FLEX CARDIO PHYSIOMONITORING SYSTEM main unit is being recalled across Canada due to a medical device issue. This recall affects users of this cardio monitoring equipment that was distributed throughout Canada. The recall is classified as Class I, indicating a serious potential health concern.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2017-12-14

Status

Closed

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/ab3ef416-6a1c-4092-8939-110f3544b0f5