Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 29263 |
| Brand Name: | Azurion MDR |
| Model: | Philips Azurion systems with Software R2.2 and R2.2.1 |
| Affected: | |
| Software version: | Philips Azurion R2.2 and R2.2.1 |
| 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: | The manufacturer has identified during internal testing that intermittently, the warm restart is not executed correctly and movement functionality remains unavailable. X-ray is available. In this situation, a new warm restart is required, which restores the system to its normal functionality. |
| Recall action type: | Correction |
| Recall action: | Software to be upgraded |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 14/4/2022 |
