Database updated: 27 October 2026

Safety Information

Medsafe Online Recall Database

Detail of Recall

Type of Product:Device
Medsafe Reference:13822
Brand Name:Beckman Coulter Access/Access2 Immunoassay Systems
Model:81600, 81600N, 386220, A69186, A25656 and A12900
Affected:
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
Brand Name:Beckman Coulter Synchron LXi 725 Clinical Systems
Model:A15642
Affected:
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
Brand Name:Beckman Coulter Unicel DxC 600i SYNCHRON Access Clinical Systems
Model:A25640
Affected:
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:Manufacturer has identified a potential problem in two pulley drive components in the mixer pulley assemblies of the above - listed systems. In some cases pulley drive components have broken parts or have become loose, mispositioned, or disconnected from their drive shafts. When these defects occur, the pulley may not turn at all, or may turn at an incorrect speed, resulting in inadequate washing or mixing of the contents of the reaction vessel.
Recall action type:Correction
Recall action:Product to be modified
Level of recall:Hospital/Pharmacy/Laboratory
Date Commenced:20/11/2012
Hide menus
Show menus
0 1 2 4 5 6 7 9 [ /