Database updated: 27 October 2026

Safety Information

Medsafe Online Recall Database

Detail of Recall

Type of Product:Device
Medsafe Reference:13889
Brand Name:Beckman Coulter Anti-Mullerian Hormone (AMH) Gen II ELISA kit
Model:Catalogue Number: A79765
Affected:All lots
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 advised that samples diluted with the AMH Gen II Sample Diluent prior to running the assay may generate results that are falsely elevated.
Recall action type:Correction
Recall action:Manufacturer to issue advice regarding use
Level of recall:Hospital/Pharmacy/Laboratory
Date Commenced:4/12/2012
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