Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 23512 |
| Brand Name: | Accelerator System, Linear - IIb - Clinac - TrueBeam - Halcyon - Unique |
| Model: | TrueBeam, TrueBeam STx, VitalBeam and EDGE treatment delivery systems. v2.0 and 2.5 [<2.5MR2] |
| 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 received reports of an anomaly that can result in a treatment without intended gating. This issue occurs when a patient planned with gating is treated on more than one TrueBeam system [includes: TrueBeam, TrueBeam STx, VitalBeam or EDGE]. |
| Recall action type: | Correction |
| Recall action: | Software to be upgraded |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 28/8/2018 |
