Database updated: 27 October 2026

Safety Information

Medsafe Online Recall Database

Detail of Recall

Type of Product:Device
Medsafe Reference:20450
Brand Name:Terumo® Advanced Perfusion System 1 Centrifugal System - Pump Stop
Model:
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 does not contain sufficient information to assist the user in the event of a centrifugal system failure. An addendum to the operator's manual to address this in the unlikely event that it occurs has been provided.
Recall action type:Correction
Recall action:Instructions for use to be updated
Level of recall:Hospital/Pharmacy/Laboratory
Date Commenced:29/7/2016
Hide menus
Show menus
0 1 2 4 5 6 7 9 [ /