Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 36597 |
| Brand Name: | Azurion |
| Model: | All Philips Azurion systems (R1.X, R2.X, R3.X, R4.0) are affected. |
| 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: | All Philips Azurion systems (R1.X, R2.X, R3.X, R4.0) are affected. |
| 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 a potential safety issue when the Reset Geometry button is configured to overwrite the table lock, while the Philips system is being used with a stand-alone third-party device or a stationary accessory not synchronized with the table (e.g., a floor-mounted device, a head stabilizer, a robotic arm with a biopsy needle). If the Reset Geometry button is then (accidentally) pressed, unintended table movement may cause the patient to move relative to the stand-alone third-party device or stationary accessory, posing a risk to the patient (e.g., if a needle is inserted into the patient). |
| Recall action type: | Correction |
| Recall action: | Software to be upgraded |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 2/3/2026 |
