Heartstart Intrepid Monitor/defibrillator
HeartStart Intrepid Monitor/Defibrillator Recall Philips is recalling HeartStart Intrepid Monitor/Defibrillator devices across Canada due to a performance issue. The device is used to monitor heart rhythm and deliver electrical therapy when needed. This is a Class I recall, indicating a serious potential health impact.
- Product
- HeartStart Intrepid Monitor/Defibrillator
- Reason
- Performance
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2023-11-17
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/2569f060-7c28-49ae-b040-f9a3706e894d