Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 20997 |
| Brand Name: | Monaco |
| Model: | |
| Affected: | Running Monaco: V 5.10.00 (including 5.10.01, 5.10.02), or V 5.11.00 (including 5.11.01), or V 5.20.00, and Using Elekta Motorized Wedges |
| 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 Inc |
| Issue: | The manufacturer has indentified that calculated dose from wedged beams can be assigned to the wrong beam. This can occur for a plan with at least two beams using the Elekta motorized wedge. The user must change the beam index numbers belonging to the two wedged beams, such that the index numbers have been exchanged for these beams, then edit the wedge angle of one of the beams. |
| Recall action type: | Correction |
| Recall action: | Manufacturer to issue advice regarding use |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 10/1/2017 |
