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 an error consisting of the sporadic appearance of a shield temperature alarm pop-up during scanning. when looking at the static temperatures everything is within specified limits. the problem is due to rf interference on the magnet supervisory cable w11234.