Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 15933 |
| Brand Name: | Elekta DesktopPRO (VMAT) |
| Model: | |
| Affected: | |
| Software version: | Desktop Pro™ R7.01 SP2 and Desktop Pro™ R4.2, R5.0, R5.1, R6.0, R6.1 |
| Recalling Organisation: | Elekta Pty Limited - New Zealand Branch Suite 302, Geyser Building, 100 Parnell Road Parnell AUCKLAND 1052 |
| Contact Information: | 0273-544-793 |
| Manufacturer: | Elekta Limited (England) |
| Issue: | During the treatment table, gantry, and collimator calibration procedures, it is possible to type incorrect values. If you do not do the quality assurance (QA) procedures after the calibration, it is possible that you will not find the error made during the calibration |
| Recall action type: | Correction |
| Recall action: | Software to be upgraded |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 10/1/2014 |
