Database updated: 27 October 2026

Safety Information

Medsafe Online Recall Database

Detail of Recall

Type of Product:Device
Medsafe Reference:15124
Brand Name:Draeger Fabius Tiro Anaesthetic Workstation
Model:
Affected:Delivered between Feb-2013 and Jul-2013
Software version:
Recalling Organisation:Draeger New Zealand Ltd
Unit 4
24 Bishop Dunn Place
East Tamaki
Auckland 2013
Contact Information:0800 559 186
Manufacturer:Draegerwerk AG & Co KGaA
Issue:Some units did not pass the high voltage final test during the final checking of the Fabius in our production facility. Investigations carried out revealed that on some power supply units from a particular batch, the required minimum clearance between an electrical component and the unit housing was not maintained. Under the influence of mechanical forces (e.g., movement of the device), this may result in small bypass currents flowing in the interior of the unit which in extreme cases cause failure of the automatic ventilation function of the device.
Recall action type:Correction
Recall action:Product to be modified
Level of recall:Hospital/Pharmacy/Laboratory
Date Commenced:13/8/2013
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