Database updated: 27 October 2026

Safety Information

Medsafe Online Recall Database

Detail of Recall

Type of Product:Device
Medsafe Reference:20497
Brand Name:Arjo Lifters - Patient Transfer - Sara 3000, Sara Plus, Maxi Twin, Maxi Compact, Maxi Move, Maxi 500, Maxi Sky 440, Maxi Sky 600, Maxi Sky 1000.
Model:Maxi Move Units
Affected:300043863 to 300100386
Software version:
Recalling Organisation:Arjo New Zealand Limited
34 Vestey Drive
Mt Wellington
AUCKLAND 1060
Contact Information:0800 000 151
Manufacturer:ArjoHuntleigh AB
Issue:Internal testing and investigative activities have confirmed that the the conductive ink which is necessary for the activation of the handset function did not meet predetermined durability requirements.
Manufacturer to perform a replacement of handset for the Maxi Move floor lifts affected by this issue.
Recall action type:Correction
Recall action:Product to be exchanged
Level of recall:Hospital/Pharmacy/Laboratory
Date Commenced:15/8/2016
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