Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 29686 |
| Brand Name: | Sensis / Sensis Lite |
| Model: | AXIOM Sensis XP, Sensis / Sensis Lite or Sensis Vibe Combo |
| 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 updated the operator manual chapter Positioning the signalinputbox for users to observe additional restrictions in instances where Signal Input Box mounting position deviates from the default position. |
| Recall action type: | Correction |
| Recall action: | Instructions for use to be updated |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 13/7/2022 |
