Database updated: 27 October 2026

Safety Information

Medsafe Online Recall Database

Detail of Recall

Type of Product:Device
Medsafe Reference:19546
Brand Name:Beckman Coulter Unicel DxH 800 Cellular Analysis System
Model:629029, B24465, B24802
Affected:
Software version:3.0.2.0
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
Brand Name:Beckman Coulter Unicel DxH SMS Cellular Analysis System
Model:775222
Affected:
Software version:3.0.2.0
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
Brand Name:Beckman Coulter Unicel DxH 600 Cellular Analysis System
Model:B23858
Affected:
Software version:1.1.1.0
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:During internal testing, Beckman Coulter determined that the software for specific systems allows the creation of multiple orders with the same Specimen Identification (ID) but different Patient Identification when manually editing pending orders at the System manager. The issue does not occur for edits of released results or for test orders requested through host transmission.
Recall action type:Correction
Recall action:Software to be upgraded
Level of recall:Hospital/Pharmacy/Laboratory
Date Commenced:9/12/2015
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