Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 20132 |
| Brand Name: | Philips Mobile Diagnost |
| Model: | WDR2 |
| 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: | Two issues: 1. The system may sporadically apply the default x-ray exposure parameters for an adult (patient type: "Normal"), even though the patient type "Newborn" was selected and is displayed in the generator control area of the Eleva User Interface. 2. Under certain conditions the detector might not be ready for examination. Released x-ray might lead to an image with artifacts and retake would be required. |
| Recall action type: | Correction |
| Recall action: | Software to be upgraded |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 6/5/2016 |
