Heartstart Mrx Defibrillator/monitor, Heartstart Mrx Defibrillator/monitor With Q-cpr, Qcpr - Cpr Meter, And Qcpr - Cpr Meter Upgrade Kit (2018-01-25)

Recall Summary Philips is recalling HeartStart MRx Defibrillator/Monitor devices and related CPR meter products distributed across Canada due to a device malfunction issue. The recall affects healthcare facilities and organizations that use these cardiac monitoring and defibrillation devices. This is classified as a Class I recall, meaning there is a serious potential health risk associated with the devices.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2018-02-09
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/7f98afcd-883d-4c42-b633-119891a198b1