Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 21463 |
| Brand Name: | Sensis / Sensis Lite |
| Model: | |
| Affected: | Sensis Vibe systems with software version VD10B |
| 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: | In Sensis Vibe systems with software version VD10B, a software error can result in: Problems generating a report and/or Information from different examinations of the same patient being combined in one report. If the erroneous report has been used for treatment or diagnosis, this can potentially result in an incorrect treatment or diagnosis. |
| Recall action type: | Correction |
| Recall action: | Software to be upgraded |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 23/5/2017 |
