Database updated: 27 October 2026

Safety Information

Medsafe Online Recall Database

Detail of Recall

Type of Product:Device
Medsafe Reference:21589
Brand Name:Coulter LH Analyzer
Model:
Affected:LH 750, LH 780, LH, 500 and HmX Analyzers
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 additional clarification for the Blast Suspect messages is necessary. In rare situations, the LH 750, LH 780, LH 500 and HmX Analyzers may not flag or detect blasts in some blood samples. This is due to limitations in the available technology as well as the properties of blasts in certain samples.
Recall action type:Correction
Recall action:Manufacturer to issue advice regarding use
Level of recall:Wholesale
Date Commenced:28/6/2017
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