Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 19955 |
| Brand Name: | Mobile Digital X Ray System |
| Model: | MobileDiagnost wDR Rel. 1 and 2 |
| 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 power plug, which has been delivered with the system is not according to the local regulation in New Zealand (AS/NZS 3115:2000). The pins of the plug can be touched when the plug is not inserted completely into the mains outlet, potentially exposing the person to electrical shock. |
| Recall action type: | Correction |
| Recall action: | Product to be exchanged |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 1/4/2016 |
