Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 33776 |
| Brand Name: | Angiographic X-Ray |
| Model: | Philips Azurion, Allura Xper and MultiDiagnost Eleva |
| Affected: | Multiple System Code |
| 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: | Azurion |
| Model: | Philips Azurion, Allura Xper and MultiDiagnost Eleva |
| Affected: | Multiple System Code |
| 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 that due to the forces applied when moving or turning the monitor of the system, the bolts and plastic parts of the Cable Hose Carriers that hold the cable hose to the monitor ceiling suspension may become loose and/or break. If this issue occurs, plastic parts and/or metal bolts of the Cable Hose Carrier(s) may fall and/or part of the cable hose may drop following the detachment of a Cable Hose Carrier. |
| Recall action type: | Correction |
| Recall action: | Product to be modified |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 17/9/2024 |
