Print version of this report
Type of Product Medical Device
TGA Recall Reference RC-2016-RN-00351-1
Product Name/Description MobileDiagnost wDR Rel1 and 2 (general purpose mobile digital x-ray system)

ARTG Number: 187112
Recall Action Level Hospital
Recall Action Classification Class II
Recall Action Commencement Date 24/03/2016
Responsible Entity Philips Electronics Australia Ltd
Reason/Issue The power plug, which has been supplied with the system, is not according to the requirements in Australia (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 a person to electrical shock.
Recall Action Recall for Product Correction
Recall Action Instructions Philips is advising users to be aware of this issue and will be replacing the plugs as a permanent fix. This action has been closed-out on 12/05/2017.
Contact Information 1800 251 400 - Philips Customer Care Centre