Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 14066 |
| Brand Name: | Philips MobileDiagnost wDR Mobile Digital X Ray System |
| Model: | All MobileDiagnost wDR without US |
| 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 failure of an electrical connection between the motor speed sensor and digital motion control board, or a related software defect, may cause the device to move with increasing speed and/or in a wrong direction. |
| Recall action type: | Correction |
| Recall action: | Product to be modified |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 14/1/2013 |
