Database updated: 27 October 2026

Safety Information

Medsafe Online Recall Database

Detail of Recall

Type of Product:Device
Medsafe Reference:15765
Brand Name:Bio-Rad D-10 dual Program Reorder Pack
Model:Catalogue Number: 220-0201
Affected:Lot Number: 20030322, 20030337, 64000081, 64000331, 64000332, 64000888, 64001344, 64002239, 64002240, 64002241
Software version:
Recalling Organisation:Bio-Rad New Zealand
Level 30
48 Shortland Street
AUCKLAND 1010
Contact Information:0508 805 500
Manufacturer:Bio-Rad Laboratories Inc
Issue:The manufacturer has received a customer report of the cartridge injection counts not being updated correctly when switching between the D-10 Dual Short Program and Extended Program on the D-10 Hemoglobin Testing System.
Recall action type:Correction
Recall action:Software to be upgraded
Level of recall:Hospital/Pharmacy/Laboratory
Date Commenced:29/11/2013
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