Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 28645 |
| Brand Name: | Azurion MDR |
| Model: | Philips Azurion 7 M20 FlexArm SW 2.0 |
| 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 will be upgrading your Azurion FlexArm system to software revision R2.2. This revision, will upgrade your system to Windows 10, includes several product enhancements and solves a number of software issue not related to risk to health to users/patients. |
| Recall action type: | Correction |
| Recall action: | Software to be upgraded |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 24/11/2021 |
