Database updated: 27 October 2026

Safety Information

Medsafe Online Recall Database

Detail of Recall

Type of Product:Device
Medsafe Reference:20449
Brand Name:Terumo Advanced Perfusion System 1, Occluder and Air Bubble Detection Module.
Model:Base for Terumo Advanced Perfusion System 1
Affected:0011-0335, 0337-0610, 1001-1034, 1037-1049, 1100, 1103-1106, 1109-1445,1447-1450
Software version:
Recalling Organisation:Terumo Australia Pty Ltd (NZ)
c/- Healthcare Logistics
56 Carrington Road
Mount Albert
Auckland 1025
Contact Information:0800 66 77 57
Manufacturer:Terumo Cardiovascular Systems Corp
Issue:The Operator's Manual is being updated with instructions on how to respond to a failure with the Occluder and Air Bubble Detection ABD Modules.
Recall action type:Correction
Recall action:Instructions for use to be updated
Level of recall:Hospital/Pharmacy/Laboratory
Date Commenced:29/7/2016
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