Product Wiki · Recalls · Health Canada — Medical Devices

Lunar Prodigy (2018-03-20) — recall 60823

Health Canada — Medical Devices · Canada · 2018-04-13 · Type II

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Agency
Health Canada — Medical Devices
Recall identifier
60823
Date of alert
2018-04-13
Country / jurisdiction
Canada
Risk level
Type II
Risk type
recall
Product category
Medical devices
Product type
Medical devices
Reported risk: Under certain conditions, when using DICOM worklist along with DICOM MPPS, a report for a bone density exam may be sent to PACS with the incorrect patient information in the DICOM header. The correct patient information will be listed on the DICOM report image; however, the report may appear under a different patient's name in the PACS.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/lunar-prodigy-2018-03-20

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