Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 28995 |
| Brand Name: | Angiographic X-Ray |
| Model: | |
| Affected: | The Philips Azurion 7 M20 systems (product code 722079) with a software R2.0.x, are 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: | 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: | 18/2/2022 |
