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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 Siemens Ltd
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