Database updated: 3 November 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 29378 |
| Brand Name: | Hemodynamic Application |
| Model: | Philips Hemodynamic Application R1.1 / R1.2.x |
| 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: | Hemodynamic Application (MDR) |
| Model: | Philips Hemodynamic Application R1.1 / R1.2.x |
| 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 |
| Issue: | We have noticed an issue with a Philips Hemodynamic Application Service Pack R1.3. Philips will be upgrading you Philips Hemodynamic Application (PHA) to service pack R1.3 |
| Recall action type: | Correction |
| Recall action: | Software to be upgraded |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 12/5/2022 |
