Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 36649 |
| Brand Name: | Hemodynamic Application (MDR) |
| Model: | Philips Interventional Hemodynamic System |
| Affected: | |
| Software version: | |
| Recalling Organisation: | Philips New Zealand Commercial Limited Level 3 123 Carlton Gore Road Newmarket AUCKLAND 1023 |
| Contact Information: | 0800 251 400 |
| Manufacturer: | Philips Medical Systems Nederland BV |
| Brand Name: | IntelliVue Patient Monitors |
| Model: | Affected systems are Philips Interventional Hemodynamic Systems with Philips Hemodynamic Application software version 1.4.1 or lower |
| Affected: | |
| Software version: | |
| Recalling Organisation: | Philips New Zealand Commercial Limited Level 3 123 Carlton Gore Road Newmarket AUCKLAND 1023 |
| Contact Information: | 0800 251 400 |
| Manufacturer: | Philips Medizin Systeme Boblingen GmbH |
| Issue: | The Philips Interventional Hemodynamic System automatically deletes the oldest case data when storage is full, but it does not remove export files, snapshots, or generated reports. These accumulate over time and can eventually fill the Hemo Host PC disk. When the disk is full, new cases cannot be opened - the application launches in review mode only. Live signals from the IntelliVue X3 will still display, but users cannot interact with the data. If the disk becomes full during an active case, data will continue to display and functionality remains, but the case will not be saved and cannot be reviewed once closed. |
| Recall action type: | Correction |
| Recall action: | Manufacturer to issue advice regarding use |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 12/3/2026 |
