Database updated: 27 October 2026

Safety Information

Medsafe Online Recall Database

Detail of Recall

Type of Product:Device
Medsafe Reference:34747
Brand Name:DxC 500i Clinical Analyzer
Model:DxC 500 AU Module w/ISE, DxC 500i, Access 2 Module, DxC 500i, DxC 500 AU Module, DxC 500i, Access 2 Module, DxC 500i
Affected:SW 1.3.0 and 1.3.2
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 the system cannot recalculate a calculated result when results are rerun within the calculated test.
Recall action type:Correction
Recall action:Software to be upgraded
Level of recall:Hospital/Pharmacy/Laboratory
Date Commenced:28/2/2025
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