Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 21925 |
| Brand Name: | Angiographic X-Ray |
| Model: | |
| Affected: | Philips Allura Xper R9 systems and Azurion R1.1 systems |
| 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: | When using the downscale option, the measurements performed with the Allura Xper R9 system or Azurion R1.1 system using the QA Basic Measurement tool will not be correctly exported to the external DICOM destination. Only these measurements when using the downscale option and exported are affected. |
| Recall action type: | Correction |
| Recall action: | Software to be upgraded |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 6/9/2017 |
