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SOMATOM Products — recall 48247

Health Canada — Medical Devices · Canada · 2013-01-07 · Type I

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Agency: Health Canada — Medical Devices
Recall identifier: 48247
Date of alert: 2013-01-07
Country / jurisdiction: Canada
Risk level: Type I
Risk type: recall
Product category: Medical devices
Product type: Medical devices
Notice status: Archived by the issuing authority — kept for reference

Reported risk: There is a highly sporadic malfunction that concerns the 3D reconstruction functionality of the SOMATOM Systems. This problem may occur during the process of a 3D reconstruction job planning and editing within a specific funtionality, while another functionality ("preview image") is activated. The problem presents itself as an error message window and the system needs to be rebooted.

Primary source: https://recalls-rappels.canada.ca/en/alert-recall/somatom-products

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SOMATOM Products — recall 48247

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