Product Wiki · Recalls · Health Canada — Medical Devices

Artis Zee Floor (2014-02-07) — recall 51375

Health Canada — Medical Devices · Canada · 2014-03-21 · Type III

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Agency
Health Canada — Medical Devices
Recall identifier
51375
Date of alert
2014-03-21
Country / jurisdiction
Canada
Risk level
Type III
Risk type
recall
Product category
Medical devices
Product type
Medical devices
Notice status
Archived by the issuing authority — kept for reference
Reported risk: An inappropriate cable connection has been assembled in Artis Zee systems with a certain serial numbers. Such an inappropriate cable connection may cause a system failure which may possibly lead to a restricted maneuverability of the gantry system. This update only affects systems of a specific production series.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/artis-zee-floor-2014-02-07

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