Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 22328 |
| Brand Name: | Phadia Prime |
| Model: | |
| Affected: | With Phadia 250, Phadia 2500E/EE and Phadia 5000E/E+E running EliA tests |
| Software version: | |
| Recalling Organisation: | Abacus ALS Limited 55b Richard Pearse Drive Airport Oaks Auckland 2022 |
| Contact Information: | 0800 222 170 |
| Manufacturer: | Phadia AB |
| Issue: | Erroneous results may occur as a result of a software issue with all versions of the Phadia Prime software up to and including version 2.1.4 connected to the Phadia 250, Phadia 2500E/EE and Phadia 5000E/E+E instruments when running EliA tests. |
| Recall action type: | Correction |
| Recall action: | Software to be upgraded |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 29/11/2017 |
