Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 36771 |
| Brand Name: | Philips Allura and Azurion Systems |
| Model: | Azurion 7 B20, Azurion 7 M12, Azurion 7 M20 |
| Affected: | Models number - 722068, 722078, 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 |
| Issue: | The manufacturer identified that the deaeration hose in CU3101 X-ray tube cooling units (manufactured February 2016–May 2020) may degrade over time, leading to oil leakage and reduced cooling performance. If oil flow drops below a threshold, the system automatically switches to low-dose fluoroscopy with a tube cooler error message, which cannot be resolved by restarting. Leaked oil is usually contained within the system, but in rare cases may escape, contact hot surfaces, and generate fumes that can activate environmental detection systems. |
| Recall action type: | Correction |
| Recall action: | Product to be exchanged |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 4/5/2026 |
