Database updated: 3 November 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 37809 |
| Brand Name: | Siemens Healthineers AG - Class IIa - GMDN 58250 |
| Model: | |
| 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 Healthineers AG |
| Brand Name: | Siemens Healthcare GmbH (MDR), MRI system |
| Model: | |
| 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 Healthineers AG |
| Issue: | A software issue has been identified in syngo.via MR Cardiac Analysis MR Flow Quantification when Beat Sensor triggering is used for retrospectively gated 2D cardiac flow examinations. The issue affects specified MAGNETOM MR and BIOGRAPH One PET/MR scanner models operating with certain software versions and licences. |
| Recall action type: | Correction |
| Recall action: | |
| Level of recall: | |
| Date Commenced: | 27/10/2026 |
