Product Wiki · Recalls · Health Canada — Medical Devices

DRX Transportable System (2013-09-11) — recall 50519

Health Canada — Medical Devices · Canada · 2013-10-16 · Type II

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Agency
Health Canada — Medical Devices
Recall identifier
50519
Date of alert
2013-10-16
Country / jurisdiction
Canada
Risk level
Type II
Risk type
recall
Product category
Medical devices
Product type
Medical devices
Notice status
Archived by the issuing authority — kept for reference
Reported risk: Carestream recently received reports of a non-diagnostic image on exams when a normal exposure mode (NEM) image is taken immediately prior to an extended exposure mode (EEM) image with the system in fast preview mode. Investigation revealed that the directview version 5.5 and 5.6 console software when used with DRX-1 detector version 69 firmware contained a timing issue which could result in a non-diagnostic image.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/drx-transportable-system-2013-

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