Database updated: 27 October 2026

Safety Information

Medsafe Online Recall Database

Detail of Recall

Type of Product:Device
Medsafe Reference:20968
Brand Name:Elekta Monaco
Model:
Affected: V 5.00.00 (including 5.00.01, 5.00.02, 5.00.03, 5.00.04), or V 5.10.00 (including 5.10.01, 5.10.02, 5.10.04), or . V 5.11.00 (including 5.11.01), or V 5.20.00, and Using the Collapsed Cone Algorithm, and . Using Varian Enhanced Dynamic Wedges (EDW) or Si
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:EDW or VW wedge files can be loaded into incorrect energies using Treatment Unit (TU) Storing. No warning or consistency checking is done for EDW or VW files when adding these to the database.
Recall action type:Correction
Recall action:Manufacturer to issue advice regarding use
Level of recall:Hospital/Pharmacy/Laboratory
Date Commenced:21/12/2016
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