Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 31757 |
| Brand Name: | Angiographic X-Ray |
| Model: | Allura Xper |
| Affected: | Potential loss of imaging functionality resulting from no or intermittent X-ray radiation initiation |
| 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: | Allura Centron |
| Model: | Allura Centron |
| 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 India Ltd |
| Brand Name: | Azurion MDR |
| Model: | Azurion 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 updated the Repair Instructions to ensure that the patient table and table cover is correctly adjusted to prevent a gap between the table cover and floor. The manufacturer has also updated its Preventative Maintenance Manual to include additional activities to help ensure the proper operation of the foot switch. |
| Recall action type: | Correction |
| Recall action: | Software to be upgraded |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 4/9/2023 |
