Heartstart Intrepid Monitor/defibrillator
HeartStart Intrepid Monitor/Defibrillator Recall Philips is recalling HeartStart Intrepid Monitor/Defibrillator devices across Canada due to a performance issue. This device is used to monitor heart rhythm and deliver electrical therapy to restore normal heart function in patients. The recall affects all HeartStart Intrepid units distributed in Canada.
- Product
- HeartStart Intrepid Monitor/Defibrillator
- Reason
- Performance
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2024-07-22
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/5d3e53da-2331-4c9d-8170-d4638d57bdf3