Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 25572 |
| Brand Name: | OmniDiagnost system |
| Model: | Velara X-ray generator of the Philips Allura Xper, the Integris, the MultiDiagnost Eleva and OmniDiagnost systems |
| 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: | Velara X-ray generator of the Philips Allura Xper, the Integris, the MultiDiagnost Eleva and OmniDiagnost systems |
| 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 that a capacitor inside the convertor of the Velara X-ray generator may fail after a large number of surges in a short period of time. When this occurs, no image acquisition is possible anymore. The failed capacitor may produce smoke and a burning odor in the room where the generator is located. If the system is a biplane model, X-ray acquisition is still possible on the other channel. If the system is a monoplane, it cannot be used anymore until the capacitor is replaced. |
| Recall action type: | Correction |
| Recall action: | Product to be modified |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 15/1/2020 |
