Database updated: 27 October 2026

Safety Information

Medsafe Online Recall Database

Detail of Recall

Type of Product:Device
Medsafe Reference:24563
Brand Name:SenTec
Model:
Affected:Multiple Lot numbers
Software version:
Recalling Organisation:Apex Medical NZ Limited
Unit 4
4 Wilk Lane
Browns Bay
Auckland 0630
Contact Information:
Manufacturer:SenTec AG
Issue:Due to a manufacturing issue of the electrolyte cartridge of certain Membrane Changer Inserts, there is an increased chance (approx. 5%) of no electrolyte or a reduced amount of electrolyte being applied to the sensor during the membrane change procedure if a MC with such an Insert is used.
Recall action type:Recall
Recall action:Manufacturer to issue advice regarding use
Level of recall:Hospital/Pharmacy/Laboratory
Date Commenced:10/5/2019
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