| 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 |
|
| 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 |