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Multidiagnost Eleva — recall 52799

Health Canada — Medical Devices · Canada · 2015-01-28 · Type II

As described by Health Canada — Medical Devices: Multidiagnost Eleva - Image Intensifier - TV Image Detector and Multidiagnost Eleva - Flat Detector - Image Detector (2015-01-20)

Compiled from an official source — the facts on this page are reproduced from the issuing authority’s own published notice, which is linked above. No AI-generated text appears on this page. How we use AI →
Agency
Health Canada — Medical Devices
Recall identifier
52799
Date of alert
2015-01-28
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: Philips Healthcare has discovered through customer complaints and internal testing an intermittent electronic product defect. In the MD Eleva system, software license keys are used to enable particular functionality. In software release r6.1.1sp2 and r6.1.2 intermittently part of the software keys are not loaded: the license key for spectral filter the license key for full table tilt range
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/multidiagnost-eleva-image-inte

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