Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 25716 |
| Brand Name: | Emicizumab medicine and factor VIII assays |
| Model: | |
| Affected: | All lots |
| Software version: | |
| Recalling Organisation: | Diagnostica Stago Pty Ltd Level 3 64 Cashel Street Christchurch |
| Contact Information: | +64 3 377 4115 |
| Manufacturer: | Diagnostica Stago SAS |
| Issue: | The manufacturer has identified when using the STA - Deficient VIII or STA - ImmunoDef VIII reagent there is a potential risk of contamination by Emicizumab of factor VIII assays on the following Stago instruments: STA® Compact, STA® Compact Max, STA-R® Evolution or STA-R® Max. |
| Recall action type: | Correction |
| Recall action: | Manufacturer to issue advice regarding use |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 17/2/2020 |
