Database updated: 27 October 2026

Safety Information

Medsafe Online Recall Database

Detail of Recall

Type of Product:Device
Medsafe Reference:26171
Brand Name:Perseus Anaesthesia Family of Devices/Systems
Model:Drager Perseus A500 Anesthesia Machine
Affected:
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:The manufacturer has become aware of isolated cases in which the Medibus interface of the Perseus A500 Anaesthesia Machine was disrupted by external non-Medibus-compliant data packages such that the internal processor became overloaded.
Recall action type:Correction
Recall action:Software to be upgraded
Level of recall:Hospital/Pharmacy/Laboratory
Date Commenced:24/6/2020
Hide menus
Show menus
0 1 2 4 5 6 7 9 [ /