Product Wiki · Recalls · Health Canada — Medical Devices

ORTHO VISION (2019-07-16) — recall 44578

Health Canada — Medical Devices · Canada · 2019-07-26 · Type II

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Agency
Health Canada — Medical Devices
Recall identifier
44578
Date of alert
2019-07-26
Country / jurisdiction
Canada
Risk level
Type II
Risk type
recall
Product category
Medical devices
Product type
Medical devices
Reported risk: Due to a software anomaly on ORTHO VISION and ORTHO VISION Max Analyzers configured with software version 5.12.3 or 5.12.4, flushing of the Pipette may occur in an unexpected location after the Pipette arm (PIPA) exits IDLE mode and moves away from the Wash Station while refilling the Liquid System (LSYS) with saline.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/ortho-vision-2019-07-16

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