Type of Product |
Medical Device |
TGA Recall Reference |
RC-2013-RN-00201-1 |
Product Name/Description |
Artis Zeego Systems (Fluoroscopic angiographic x-ray system)
ARTG Number: 102177 |
Recall Action Level |
Hospital |
Recall Action Classification |
Class III |
Recall Action Commencement Date |
5/03/2013 |
Responsible Entity |
|
Reason/Issue |
After a functional check of the brakes on the Artis Zeego system, there is a possibility of any output system information being overlaid and obscured with different system information. The overlaid information requests users to contact the service department. |
Recall Action |
Recall for Product Correction |
Recall Action Instructions |
If after carrying out the regular brake test, the system can persistently only be moved at a reduced speed, customers are requested to notify the customer care centre. A software update will be implemented to prohibit information from being overlaid. |
Contact Information |
1800 310 300 - Siemens Healthcare Quality Management |