Database updated: 27 October 2026

Safety Information

Medsafe Online Recall Database

Detail of Recall

Type of Product:Device
Medsafe Reference:26160
Brand Name:Alinity m System
Model:
Affected:Serial number - 00164, 00197, 00200
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
Issue:The pipettor error may cause a potential delay in the generation of results. The RV popping may result in an unrecoverable error, placing the ADU out of service or stopping the process of transferring RVs for waste disposal and sending samples to exception.
Recall action type:Correction
Recall action:Software to be upgraded
Level of recall:Hospital/Pharmacy/Laboratory
Date Commenced:22/6/2020
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