Database updated: 27 October 2026

Safety Information

Medsafe Online Recall Database

Detail of Recall

Type of Product:Device
Medsafe Reference:37092
Brand Name:DxC 500i Clinical Analyzer
Model:DxC 500 AU Module w/ISE, DxC 500i and DxC 500 AU Module, DxC 500i
Affected:Reference: C63522, C63521 - Software: 1.5 or lower
Software version:
Recalling Organisation:Beckman Coulter NZ Ltd
Suite 2, Level 4
30 St Benedicts Street
Newton
AUCKLAND
Contact Information:0800 446 109
Manufacturer:Beckman Coulter Inc
Issue:The manufacturer has determined that a modification made by operators to the below 25 predefined calculated rules, which are included as part of the parameter package, will revert to the default expression following parameter package or software upgrades.
Recall action type:Correction
Recall action:Software to be upgraded
Level of recall:Hospital/Pharmacy/Laboratory
Date Commenced:16/7/2026
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