Database updated: 27 October 2026

Safety Information

Medsafe Online Recall Database

Detail of Recall

Type of Product:Device
Medsafe Reference:23978
Brand Name:MOSAIQ
Model:Using release version 1.0 and higher and Multi-ACCESS using release version 6.1 and higher.
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:Elekta Inc
Issue:If there are no Wedge IDs included in the DICOM RT PLAN sent from the TPS, the field in MOSAIQ will be created with no wedge. If not discovered, treatment of a field without the planned wedge will receive more dose than the treatment plan indicates.
Recall action type:Correction
Recall action:Software to be upgraded
Level of recall:Hospital/Pharmacy/Laboratory
Date Commenced:13/12/2018
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