Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 21959 |
| Brand Name: | Artis Q, Q.zen, zeego, zee systems |
| Model: | |
| Affected: | Lot number – 10094137, 10848281, 10848282, 10848280, 10848283, 10094135, 10094139, 10848355, 10280959, 10848353 |
| 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: | In the application "DSA Roadmap" the Artis system's intended behavior is to reject the stored Vesselmap from previously acquired DSA if the patient table was moved during the Roadmap workflow. In rare cases the system does not reject the DSA Vesselmap and uses it for the further Roadmap workflow steps. Depending on the amount of table movement which was applied during the Roadmap workflow, the DSA Vesselmap might be overlaid as vessel tree at a position which does not fulfill the requirements for accuracy. |
| Recall action type: | Correction |
| Recall action: | Software to be upgraded |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 12/9/2017 |
