Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 13282 |
| Brand Name: | Elekta Apex |
| Model: | All models |
| Affected: | All versions |
| 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: | The Agility beam limiting device (BLD) does not support the use of Apex at this time. Apex has not been integrated or classified as compatible for use with the Agility. |
| Recall action type: | Correction |
| Recall action: | Instructions for use to be updated |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 6/8/2012 |
