Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 25552 |
| Brand Name: | Ysio Max |
| Model: | Ysio Max – 10762470 |
| 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 |
| Brand Name: | Luminos & Multitom Rax |
| Model: | Luminos Agile Max - 10762472, Luminos dRF Max – 10762471 |
| 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 |
| Brand Name: | UROSKOP Omnia Max |
| Model: | UROSKOP Omnia Max – 10762473 |
| 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: | Issue 1.The manufacturer has received a report of a system collision due to inappropriate use of the bypass key which is overriding the built-in collision control. The bypass key is intended to enable moving an otherwise blocked system only to avert an immediate hazard. Issue 2. The manufacturer has received a report of an image which was assigned to two different patients. |
| Recall action type: | Correction |
| Recall action: | Software to be upgraded |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 9/1/2020 |
