Product Wiki · Recalls · Health Canada — Medical Devices

ERGO++ RTP SOFTWARE (2017-09-27) — recall 57158

Health Canada — Medical Devices · Canada · 2017-10-06 · Type II

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Agency
Health Canada — Medical Devices
Recall identifier
57158
Date of alert
2017-10-06
Country / jurisdiction
Canada
Authority classification
Type II
Notice type
recall
Product category
Medical devices
Product type
Medical devices
Notice status
Archived by the issuing authority — kept for reference
Reported risk: Elekta has become aware of the potential for incorrect DICOM mapping of the exported collimator or couch angles from ERGO, which would lead to incorrect rotation of the collimator or couch when using a MLC device for planning.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/ergo-rtp-software-2017-09-27

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