Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 37758 |
| Brand Name: | Philips Allura Xper FD Angiographic X-Ray |
| Model: | Philips Allura Xper R8.1.x and R8.2.x systems with FlexVision monitor |
| 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 software issue that may cause the FlexVision software application to become unresponsive during clinical use. When this occurs, the FlexVision monitor may either: · turn blank and no longer display live images or other information shown on the FlexVision monitor; or · freeze on the last displayed screen and no longer update live images or other information shown on the FlexVision Monitor. A cold system restart is required to restore normal FlexVision display functionality. |
| Recall action type: | Correction |
| Recall action: | Software to be upgraded |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 21/10/2026 |
