Database updated: 27 October 2026

Safety Information

Medsafe Online Recall Database

Detail of Recall

Type of Product:Device
Medsafe Reference:24612
Brand Name:Abbott ARCHITECT Assays
Model:ARCHITECT Complement C3, ARCHITECT Immunoglobulin A, ARCHITECT Immunoglobulin G, ARCHITECT Immunoglobulin M, ARCHITECT Apolipoprotein A1,ARCHITECT Complement C4, ARCHITECT Haptoglobin,ARCHITECT Apolipoprotein B,ARCHITECT Transferrin
Affected:
Software version:
Recalling Organisation:Abbott Diagnostics Division
Ground Floor, Building D
4 Pacific Rise
Mt Wellington
AUCKLAND 1640
Contact Information:0800 656 233
Manufacturer:Abbott Diagnostics Division
Issue:There is a potential for falsely depressed results due to fibrinogen interference with EDTA specimens for multiple ARCHITECT Assays. For Complement C4, there is a potential for falsely depressed results due to fibrinogen interference with heparin tubes.
Recall action type:Correction
Recall action:Manufacturer to issue advice regarding use
Level of recall:Hospital/Pharmacy/Laboratory
Date Commenced:23/5/2019
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