Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 22989 |
| Brand Name: | Medical Intelligence HexaPOD evo RT System |
| Model: | HexaPOD evo Module. |
| Affected: | |
| 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: | Medical Intelligence Medizintechnik GmbH |
| Issue: | It has been noted that upon completion of a 6D workflow, the HexaPOD evo Module may be in a tilted state, if it is moved to the position used for 3D (non-iGUIDE) treatments. In a subsequent 3D workflow, a possible incorrect position of the patient, due to a tilt of the HexaPOD, may be difficult to detect without verification (e.g. imaging). This description is not relevant for an iGUIDE workflow (6D). The problem occurs only when you switch from a 6D to a 3D workflow without iGUIDE. |
| Recall action type: | Correction |
| Recall action: | Manufacturer to issue advice regarding use |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 17/5/2018 |
