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 distal end of certain lots of terumo medical destination products may not contain the labeled 5cm of coating. while there have been no complaints or patient related incidents reported the lack of coating couls render it difficult to navigate the device to the target vasculature.