Database updated: 27 October 2026

Safety Information

Medsafe Online Recall Database

Detail of Recall

Type of Product:Device
Medsafe Reference:27079
Brand Name:ORTHO VISION
Model:ORTHO VISION® and ORTHO VISION® Max Analyzers configured with software version 5.12.8 or 5.13.0
Affected:
Software version:
Recalling Organisation:Ortho-Clinical Diagnostics
c/o Quigg Partners
Level 7, 36 Brandon Street
Wellington 6011
Contact Information:0800 402 899
Manufacturer:Ortho-Clinical Diagnostics Inc
Issue:Due to a software anomaly on ORTHO VISION® and ORTHO VISION® Max Analyzers configured with software version 5.12.8 or 5.13.0, flushing of the Pipette may occur in a reagent vial after the Pipette arm (PIPA) exits IDLE mode , one or more reagent/diluent vials are loaded on the system and the operator enters Maintenance Mode before the Analyzer completes the reagents inventory.
Recall action type:Correction
Recall action:Software to be upgraded
Level of recall:Hospital/Pharmacy/Laboratory
Date Commenced:21/12/2020
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