Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 18689 |
| Brand Name: | Philips MobileDiagnost wDR1 and 2, resistive arrestor strap |
| Model: | Models: wDR1 and wDR2 |
| Affected: | All MobileDiagnost wDR 1 with serial number lower than 15000005 and all MobileDiagnost wDR 2 with serial number lower than 15100050 |
| 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: | When the system is driven over a non-conductive floor and then over a conductive, grounded part, proper control of the drive behavior may not be possible. The system can be stopped by releasing the drive handle. Proper behavior is re-enabled when the system is rebooted. |
| Recall action type: | Correction |
| Recall action: | Product to be modified |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 17/6/2015 |
