Database updated: 27 October 2026

Safety Information

Medsafe Online Recall Database

Detail of Recall

Type of Product:Device
Medsafe Reference:29498
Brand Name:Citadel Floatation Therapy System
Model:Arjo Citadel Patient Care Systems
Affected:
Software version:
Recalling Organisation:Arjo New Zealand Limited
34 Vestey Drive
Mt Wellington
AUCKLAND 1060
Contact Information:0800 000 151
Manufacturer:ArjoHuntleigh AB
Issue:The manfacturer has observed that the e-bay box might overheat while the device is plugged into mains. This overheating can happen when the grounding screw inside the e-bay boxis touching the inner side ofthe e-bay box cover.This can lead then to electric circuit closure ande-bay box overheating
Recall action type:Correction
Recall action:Product to be modified
Level of recall:Hospital/Pharmacy/Laboratory
Date Commenced:2/6/2022
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