Database updated: 27 October 2026

Safety Information

Medsafe Online Recall Database

Detail of Recall

Type of Product:Device
Medsafe Reference:26563
Brand Name:Perseus Anaesthesia Family of Devices/Systems
Model:
Affected:Gas Detection Module PGM and software version 2.03
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 a case in which use of software version 2.03 on the Perseus A500 Anaesthesia Machine with the PGM Gas Detection Module resulted in no inspiratory or expiratory anesthetic gas concentration being displayed at the start of surgery for several minutes.
Recall action type:Correction
Recall action:Product to be exchanged
Level of recall:Hospital/Pharmacy/Laboratory
Date Commenced:15/9/2020
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