Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 22332 |
| Brand Name: | iViewGT |
| Model: | |
| Affected: | All Digital Accelerators with iViewGT |
| 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) |
| Brand Name: | XVI 4.5 |
| Model: | |
| Affected: | All Digital Accelerators with XVI |
| 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 manufacturer has identified that if the microswitch in the PCB assembly, solenoid limit switch of the middle arm is not set up correctly, it is possible to get an uncontrolled extension of MV or kV detector arms. When the detector arm is fully extended there is no risk. |
| Recall action type: | Correction |
| Recall action: | Product to be modified |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 30/11/2017 |
