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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There is a tolerance issue on a certain production batch from april 2010. the result is that the heel of the blade may be too wide to be inserted into the head of laryngoscope handles manufactured to the "green standard".