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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Intuitive surgical inc observed an electronics subsystem failure that resulted in partial intermittent closure of the instrument grip (is2000 system). a software coding error in p7 caused the error for the mtm grip.