Philips Hemodynamic Application
Philips Hemodynamic Application Recall The Philips Hemodynamic Application software is being recalled in Canada due to a performance issue. This application is used to monitor and analyze blood flow and pressure measurements in patients. The recall affects all users of this software across Canada and has been classified as a Class I recall, indicating a serious problem.
- Product
- Philips Hemodynamic Application
- Reason
- Performance
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2024-05-16
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/f4eb7f8e-5d8a-4ba3-8aaf-1762505c690c