Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 26851 |
| Brand Name: | Artis Q, Q.zen, zeego, zee systems |
| Model: | Artis zee/ Q/ Q.zen systems with software version VD11C, VD11D and VD11E |
| Affected: | |
| 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: | If fluoroscopy exam set parameters like frame rate, pulse rate or zoom parameters are changed during a procedure while keeping the fluoroscopy pedal of the footswitch pressed, the patient entrance dose rate (Air Kerma Rate, AKR) may exceed regulatory limits. |
| Recall action type: | Correction |
| Recall action: | Manufacturer to issue advice regarding use |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 5/11/2020 |
