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Type of Product Medical Device
TGA Recall Reference RC-2015-RN-00261-1
Product Name/Description Artis Q/Q.zen systems

All lot numbers

ARTG number: 102177
Recall Action Level Hospital
Recall Action Classification Class II
Recall Action Commencement Date 19/03/2015
Responsible Entity Siemens Ltd
Reason/Issue It is possible that an electrical connection in the equipment cabinet has not been installed correctly. In potential fault scenarios (e.g. if several live wires become defective) and under certain conditions, this may prevent a safety mechanism on the system side from taking effect, thus compromising the electrical safety of the system.
Recall Action Recall for Product Correction
Recall Action Instructions Siemens is inspecting and correcting any affected units. This action has been closed-out on 1/06/2016.
Contact Information 1800 310 300 - Siemens Technical Support Centre