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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A gap in the housing of the wireless foot switch can result in liquids penetrating the interior. such liquids may include disinfection and cleaning agents but also bodily fluids. this can result in a failure of the foot switch. only wireless footswitches are affected which were delivered with artis systems after january 1 2005.