Database updated: 27 October 2026

Safety Information

Medsafe Online Recall Database

Detail of Recall

Type of Product:Device
Medsafe Reference:22252
Brand Name:LIFEPAK Defibrillator Electrode, Single-Use
Model:
Affected:Lot Number 713609
Software version:
Recalling Organisation:Medxus Ltd
Unit 4
100 Fitgerald Avenue
Christchurch 8011
Contact Information:03 365 7403
Manufacturer:Physio-Control Corporation
Issue:The artwork on the defibrillation electrodes, does not meet Physio- Control's specifications. They show incorrect electrode placement for an infant. There is no issue with the performance or function of the defibrillation electrodes; this is limited to incorrect artwork on the defibrillation electrodes within the packaging.
Recall action type:Recall
Recall action:Product to be exchanged
Level of recall:Hospital/Pharmacy/Laboratory
Date Commenced:14/11/2017
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