Heartstart Mrx Defribrillator/monitor (2019-05-27)
HeartStart MRx Defibrillator/Monitor Recall Philips is recalling HeartStart MRx defibrillator/monitor devices distributed across Canada due to a medical device issue. The recall is classified as Class I, meaning the device could cause serious injury or death. This recall affects all HeartStart MRx units currently in use in Canadian healthcare settings.
- Reason
- Medical devices
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2019-06-07
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/ede7dae1-d9b9-48b4-b8aa-ade9982a46b6