Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 29014 |
| Brand Name: | CombiDiagnost R90, ProxiDiagnost N90 (MDR) |
| Model: | |
| Affected: | Philips CombiDiagnost R90 and ProxiDiagnost N90 with software 1.1.1 or higher |
| 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 DMC GmbH |
| Brand Name: | CombiDiagnost R90 |
| Model: | |
| Affected: | Philips CombiDiagnost R90 and ProxiDiagnost N90 with software 1.1.1 or higher |
| 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 DMC GmbH |
| Issue: | The manufacturer has identified that while performing a fluoroscopy examination, there is a potential for the Radio Fluoroscopy (RF) viewer to also display a previous patient's radiography images. The problem occurs when CombiDiagnost R90 and ProxiDiagnost N90 system is using software version 1.1.1 or higher. |
| Recall action type: | Correction |
| Recall action: | Software to be upgraded |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 24/2/2022 |
