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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The reason for this recall is to inform users about user errors and specific workflow scenarios on cancelled procedures that might result in an interrupted reporting workflow. this may lead to delayed diagnosis and treatment which in the worst case might result in no or inefficient treatment.