Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 14944 |
| Brand Name: | Elekta Digital Accelerators |
| Model: | All Digital Accelerators with Electrons and Beam Modulator, MLCi/MLCi2, Agility or Asymmetric Heads |
| Affected: | All serial numbers |
| Software version: | |
| 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: | Elekta is aware that some Digital Accelerators have increased electron applicator auto-tracking settings in the field, to values greater than the factory-set defaults. Increasing auto-tracking values from factory-set defaults goes against Elekta recommendations and can result in the system becoming non-compliant with IEC standards, in particular with the safety standard IEC 60601-2-1. |
| Recall action type: | Correction |
| Recall action: | Software to be upgraded |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 5/7/2013 |
