Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 36548 |
| Brand Name: | [MDR] Azurion |
| Model: | |
| 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: | Potential loss of imaging (X-ray) functionality, and/or loss of motorized movement, and/or incorrect image content, and/or loss of data which may result in a delay or termination of procedure and/or procedural complications |
| Recall action type: | Correction |
| Recall action: | |
| Level of recall: | |
| Date Commenced: | 16/2/2026 |
