Product Wiki · Recalls · Health Canada — Medical Devices

Elekta UNITY (2019-06-12) — recall 60016

Health Canada — Medical Devices · Canada · 2019-07-19 · Type II

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Agency
Health Canada — Medical Devices
Recall identifier
60016
Date of alert
2019-07-19
Country / jurisdiction
Canada
Risk level
Type II
Risk type
recall
Product category
Medical devices
Product type
Medical devices
Reported risk: If the Set To Work (STW) phase 2 of the installation is not conducted in the correct order, the MR to MV offset values cannot be exported to the EQ database at STW phase 2 and (0,0,0) values are set instead by software installer in order to run clinical workflow tests.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/elekta-unity-2019-06-12

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