Product Wiki · Recalls · Health Canada — Medical Devices

Atellica IM 1600 Analyzer (2018-12-12) — recall 59008

Health Canada — Medical Devices · Canada · 2019-01-09 · Type III

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Agency
Health Canada — Medical Devices
Recall identifier
59008
Date of alert
2019-01-09
Country / jurisdiction
Canada
Risk level
Type III
Risk type
recall
Product category
Medical devices
Product type
Medical devices
Reported risk: Siemens healthcare diagnostics is informing customers that the Atellica Solution Software (SW) version 1.16 (SMN 11316682) may generate motion errors during reagent scanning at the IM analyzer, after a system reboot, following a mechanics off state, or when exiting the diagnostics state after the reagent compartment shutter has been opened.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/atellica-im-1600-analyzer-2018

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