Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 25564 |
| Brand Name: | ARCADIS Avantic/Orbic/Varic, Cios Connect & Siremobile Compact |
| Model: | Catalogue number – 10308193, 10308192, 11105200, 10308194 |
| 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 |
| Brand Name: | Cios Alpha / Fusion |
| Model: | Catalogue number – 10308193, 10308192, 11105200, 10308194 |
| 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: | The manufacturer has identified that if examination will exceed a total radiation time longer than 54 minutes, values of accumulated DAP and accumulated Air Kerma will not be added and be saved in radiation report before closing your studies, in detail: each of those two relevant fields will remain empty. Each single dose value of DAP and Air Kerma is not affected to this restriction and will be added correctly in your radiation report with no matter how long radiation time has been taken. |
| Recall action type: | Correction |
| Recall action: | Software to be upgraded |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 13/1/2020 |
