Database updated: 27 October 2026

Safety Information

Medsafe Online Recall Database

Detail of Recall

Type of Product:Device
Medsafe Reference:19782
Brand Name:Terumo CDI H/C Cuvette
Model:6914
Affected:Lot No TH13
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 CDI H/S Cuvette may not make a proper connection to the CDI H/S Probe.
Recall action type:Correction
Recall action:Manufacturer to issue advice regarding use
Level of recall:Hospital/Pharmacy/Laboratory
Date Commenced:23/2/2016
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