Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 24576 |
| Brand Name: | Siemens Creatine Kinase on the ADVIA Chemistry platform |
| Model: | |
| Affected: | Affected lot numbers 465336, 465663, 468449 |
| 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 Diagnostics Inc |
| Issue: | The manufacturer has received complaints indicating an increased incidence of system generated (U, u) flags on Calibration, Quality Control and patient results when using the ADVIA Chemistry Creatine Kinase (CK_L) reagent kit on the ADVIA® 1800, 2400, and XPT Chemistry Systems. Patient results with u flags are not reportable. |
| Recall action type: | Recall |
| Recall action: | Product to be destroyed |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 13/5/2019 |
