Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 29172 |
| Brand Name: | Angiographic X-Ray |
| Model: | Azurion 3 M12 722063, Azurion 7 B12 722067, Azurion 3 M15 722064 Azurion 7 B20 722068, Allura Xper R9 7 M12 722065 Azurion 7 M12 722078, Allura Xper R9 7 M20 722066 Azurion 7 M20 722079 |
| 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 become aware that the Azurion system, the user can add a new study to a patient by selecting the option Add Study. The Add Study dialogue box is then displayed where the Patient Type is selected to perform the study. Due to a software defect, when the study is initiated by pressing Start Procedure, the Patient Type changes inadvertently to a Patient Type different than the one selected |
| Recall action type: | Correction |
| Recall action: | Software to be upgraded |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 25/3/2022 |
