Canadian data is current through March 2018. All of the data comes from Health Canada, except for the categories Manufacturer Parent Company and Product Classification.
The Parent Company and the Product Classification were added by ICIJ.
The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and Canada.
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For a specific number of artis zee/q biplane systems a screw connection in the ceiling mount consisting of 12 screws might not have been attached and fastened according to the quality standards. the connection is located within the rotation unit of the second plane.