Database updated: 27 October 2026

Safety Information

Medsafe Online Recall Database

Detail of Recall

Type of Product:Device
Medsafe Reference:20499
Brand Name:Terumo Advanced Perfusion System 1
Model:801764
Affected:
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:Reports have been received of issues that manifest themselves as power or communications failures in the system network. Terumo's investigation revealed an internal cable with an inadequate crimp was installed in a subset of the total population of Terumo System 1 units. The poor crimp in the cable can create a loss or degradation of internal power on one side of the system's base.
Recall action type:Correction
Recall action:Instructions for use to be updated
Level of recall:Hospital/Pharmacy/Laboratory
Date Commenced:15/8/2016
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