Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 28651 |
| Brand Name: | Sensis / Sensis Lite |
| Model: | |
| Affected: | Catalogue number – 11007641 |
| 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 under certain sporadic circumstances it can happen that on a Sensis Vibe Hemo system with VD12A software the CO (Cardiac Output) measurement using the Thermodilution method will temporarily no longer be possible. |
| Recall action type: | Correction |
| Recall action: | Software to be upgraded |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 26/11/2021 |
