Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 17300 |
| Brand Name: | Philips mobileDiagnost wDR Digital X Ray System |
| Model: | |
| Affected: | All units |
| 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: | If the system drives over insulated flooring or carpeting and then over an uninsulated, electrically grounded section, an electrostatic discharge can cause the system's Digital Motion Control (DMC) board to malfunction, resulting in unintended movement of the system, e.g., an increase in speed or a change of direction. |
| Recall action type: | Correction |
| Recall action: | Product to be modified |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 5/9/2014 |
