Database updated: 27 October 2026

Safety Information

Medsafe Online Recall Database

Detail of Recall

Type of Product:Device
Medsafe Reference:20534
Brand Name:Base for Terumo Advanced Perfusion System
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:Manufacturer has received reports of the Central Control Monitor (CCM) for Terumo Advanced Perfusion System 1 losing partial or full functionality. Symptoms that have been associated with a malfunctioning CCM include: full or partial loss of display; loss of control functions; or an inability to distinguish various status, alert, or alarm conditions. In one report, the CCM emitted smoke. Although the occurrence for a CCM malfunction is unlikely, the possible risks of malfunction range from negligible to very severe.
Recall action type:Correction
Recall action:Instructions for use to be updated
Level of recall:Hospital/Pharmacy/Laboratory
Date Commenced:19/8/2016
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