Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 35776 |
| Brand Name: | Azurion |
| Model: | 722068 Azurion 7 B20, 722079 Azurion 7 M20, 722228 Azurion 5 M20 |
| 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: | Angiographic X-Ray |
| Model: | Philips Azurion R2.x or R3.x systems. |
| 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: | The manufacturer has identified that the firewall router might not be installed in specific Azurion systems. The firewall router separates the internal Azurion network from the hospital network. If this router is not installed, there could be interference between the Azurion and the hospital network. When this occurs, the Azurion will initiate an automatic restart of the positioning software, during which all motorized movements will be disabled and the message The geometry is restarting will be displayed on the screen. The restart will take approximately 90 seconds to complete, after which motorized movements will be fully available. X-ray imaging is not impacted by this issue and remains available during the positioning software restart. |
| Recall action type: | Correction |
| Recall action: | Software to be upgraded |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 11/9/2025 |
