Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 33478 |
| Brand Name: | Angiographic X-Ray |
| Model: | Philips Azurion System R1.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: | The manufacturer has identified two issues in software version R1.x of the Philips Azurion system that may affect: 1. Management of the system Log Trace Files 2.Time to Perform a Cold Restart Note: This issue only impacts the Philips Azurion R1.x systems that are currently connected to Philips Remote Service or that were connected in the past. |
| Recall action type: | Correction |
| Recall action: | Software to be upgraded |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 26/7/2024 |
