Database updated: 27 October 2026

Safety Information

Medsafe Online Recall Database

Detail of Recall

Type of Product:Device
Medsafe Reference:21581
Brand Name:Artis Q, Q.zen, zeego, zee systems
Model:
Affected:Catalogue number 5904441, 7728392, 7412807, 7413078, 7008605, 7555357, 7555373, 7727717, 10094141, 10094135, 10094137, 10280959, 10848281, 10848280, 10848283, 10848282 with Artis table
Software version:
Recalling Organisation:Siemens Healthcare (NZ) Ltd
Millennium Centre, Part Level 2, Building A
600 Great South Road
Ellerslie
AUCKLAND 1051
Contact Information:0800 310 300
Manufacturer:Siemens Healthcare GmbH
Brand Name:Artis one
Model:
Affected:Catalogue number 5904441, 7728392, 7412807, 7413078, 7008605, 7555357, 7555373, 7727717, 10094141, 10094135, 10094137, 10280959, 10848281, 10848280, 10848283, 10848282 with Artis table
Software version:
Recalling Organisation:Siemens Healthcare (NZ) Ltd
Millennium Centre, Part Level 2, Building A
600 Great South Road
Ellerslie
AUCKLAND 1051
Contact Information:0800 310 300
Manufacturer:Siemens Shenzhen Magnetic Resonance Ltd
Brand Name:ARCADIS Avantic/Orbic/Varic, Cios Connect & Siremobile Compact
Model:
Affected:Catalogue number 5904441, 7728392, 7412807, 7413078, 7008605, 7555357, 7555373, 7727717, 10094141, 10094135, 10094137, 10280959, 10848281, 10848280, 10848283, 10848282 with Artis table
Software version:
Recalling Organisation:Siemens Healthcare (NZ) Ltd
Millennium Centre, Part Level 2, Building A
600 Great South Road
Ellerslie
AUCKLAND 1051
Contact Information:0800 310 300
Manufacturer:Siemens Healthcare GmbH
Issue:Large amount of liquid can enter the table. This may result in electric table movement failure.
Recall action type:Correction
Recall action:Product to be modified
Level of recall:Hospital/Pharmacy/Laboratory
Date Commenced:23/6/2017
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