Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 25540 |
| Brand Name: | Accelerator System, Linear - IIb - Clinac - TrueBeam - Halcyon - Unique |
| Model: | TrueBeam®, VitalBeam® Radiotherapy System, or EDGE® RadioSurgery System |
| Affected: | |
| Software version: | |
| Recalling Organisation: | Varian Medical Systems Australasia Pty Ltd (NZ) Millenium Centre, Level 3, Building C, 600 Great South Road Ellerslie Auckland 1051 |
| Contact Information: | 0800 486 732 |
| Manufacturer: | Varian Medical Systems Inc |
| Issue: | The manufacturer has discovered an anomaly that may occur when a patient treatment plan with one or more Enhanced Dynamic Wedge (EDW) fields is loaded on the TrueBeam, VitalBeam or EDGE system version 2.5 or 2.7. |
| Recall action type: | Correction |
| Recall action: | Manufacturer to issue advice regarding use |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 8/1/2020 |
