Database updated: 27 October 2026

Safety Information

Medsafe Online Recall Database

Detail of Recall

Type of Product:Device
Medsafe Reference:36561
Brand Name:Mobile Digital X Ray System
Model:Philips MobileDiagnost wDR
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:If excessive liquid is used during cleaning of the MobileDiagnost wDR system, fluid can enter the handgrip button edges and cause corrosion or an electrical short at the overlay connector. This may result in unintended slow movement of the system (20 cm/s), controlled by the four handgrip motion buttons. At this low speed, users or bystanders can easily move away, and the system can be stopped using the Emergency Stop button. The issue resolves once the liquid dries.
Recall action type:Correction
Recall action:Software to be upgraded
Level of recall:Hospital/Pharmacy/Laboratory
Date Commenced:17/2/2026
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