Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 25979 |
| Brand Name: | syngo MR |
| Model: | |
| Affected: | Material number(s): 10091637 |
| 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 when importing the measurements from an ultrasound system and remeasuring them on a workstation, the measurements from the ultrasound system and workstation could be averaged. The problem is limited to supported syngo Dynamics versions using cardiac ultrasound package and DICOM SR (structured reporting) import. 2. When importing fetal echo measurements from DICOM SR (structured reporting) CD38 and CD39 to syngo Dynamics VA20F and VA20G, fetus measurements are not stored on an individual fetus basis. Instead, all fetus measurements and derived results are combined and stored as study level data. |
| Recall action type: | Correction |
| Recall action: | Software to be upgraded |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 29/4/2020 |
