Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 28847 |
| Brand Name: | Mobile Digital X Ray System |
| Model: | MobileDiagnost wDR - 712002, 712004, 712006, 712007, 712087 |
| 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 DMC GmbH |
| Issue: | The manufacturer has identified that if liquid comes in contact with the capacitive touch screen, specifically the action buttons that modulate kV, mA, ms, mAs values, there is a potential of additional radiation due to change in exposure parameters. |
| Recall action type: | Correction |
| Recall action: | Manufacturer to issue advice regarding use |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 17/1/2022 |
