Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 25500 |
| Brand Name: | Angiographic X-Ray |
| Model: | Philips VesselNavigator application when used with the Philips Azurion System R1.2.x and R2.0.x |
| 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 a Digital Subtracting Angiography (DSA) is exported to the VesselNavigator application, the DSA is displayed without subtraction. The unsubtracted images contain more anatomical information than the DSA, which may not be suitable for verification of the registration of a pre-operative CT/MR with X-ray images during the Live Guidance step. |
| Recall action type: | Correction |
| Recall action: | Software to be upgraded |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 19/12/2019 |
