Heartstart Mrx Defibrillator/monitor (2017-02-27)
Heartstart MRx Defibrillator/Monitor Recall Philips is recalling certain Heartstart MRx defibrillator/monitor devices distributed across Canada due to a device malfunction issue. The recall is classified as Class I, meaning there is a serious risk of adverse health consequences. This recall affects users of the affected Heartstart MRx models in Canada.
- Reason
- Medical devices
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2017-03-16
- Status
- Closed
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/9958b981-294b-4642-96e7-586ffe4b501a