Database updated: 3 November 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 37822 |
| Brand Name: | Angiographic X-Ray |
| Model: | Azurion 7 M20 |
| Affected: | System code: 722079 |
| 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: | [MDR] Azurion |
| Model: | Azurion 7 M20 |
| Affected: | System code: 722224 |
| 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 identified that, during certain repair or service activities on Azurion systems, SSDs not specified in the Medical Device File may have been installed. These SSDs may have different performance characteristics and potentially reduced reliability over time. If an affected SSD fails to perform as intended, this may result in loss of imaging or motorised movement functionality, a blank/black display, inability to store newly acquired images, or inability to access previously acquired images. |
| Recall action type: | Correction |
| Recall action: | Software to be upgraded |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 28/10/2026 |
