Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 26001 |
| Brand Name: | VITEK® 2 8 01 |
| Model: | EndofDay process for VITEK ® 2 Systems Software Version 8.01. |
| Affected: | |
| Software version: | |
| Recalling Organisation: | Medi'Ray New Zealand Ltd 53-55 Paul Matthews Road Albany Auckland 0632 |
| Contact Information: | 0800 633 472 |
| Manufacturer: | BioMerieux Inc |
| Issue: | The manufacturer has confirmed a software anomaly associated with the nightly EndofDay process for VITEK ® 2 Systems Software Version 8.01. This anomaly, which occurs only after the VITEK® 2 8.01 software database has reached its 20MB capacity of data, prevents the database backup that is scheduled to occur as part of the EndofDay process from completing. |
| Recall action type: | Correction |
| Recall action: | Software to be upgraded |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 5/5/2020 |
