Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 21091 |
| Brand Name: | Siemens ADVIA® Centaur XPT |
| Model: | |
| Affected: | software V1.0.1, V1.0.2, V1.0.3, V1.1, V1.2 |
| Software version: | |
| Recalling Organisation: | Siemens Healthcare (NZ) Ltd 55 Hugo Johnston Drive Penrose Auckland |
| Contact Information: | 0800 310 300 |
| Manufacturer: | Siemens Healthcare Diagnostics Inc |
| Issue: | The manufacturer has identified multiple software issues for all the ADVIA® Centaur XPT system software versions V1.0.1 (Bundle 1.0.912 SMN 10819704), V1.0.2 (Bundle 1.0.1086 SMN 11219806), V1.0.3 (Bundle 1.0.1108 SMN 11220781, 11219656), V1.1 (Bundle 1.1.243 SMN 11221979, 11222064) and V1.2 (Bundle: 1.2.223.0 SMN: 11222258, 11223813)). These issues may affect the operation and workflow of the system. Follow up 11 May 2018: This follow-up communication contains important information for ADVIA Centaur XPT customers who may have received the Software Version 1.3 Release Notes (SMN 11313041 Rev. 01) and may continue to experience the System Status Unknown, LAS Communication, and 'No Primary' Error. These issues may affect the operation and workflow of the system. |
| Recall action type: | Correction |
| Recall action: | Manufacturer to issue advice regarding use |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 11/5/2018 |
