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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A batch of isoline defibrillation leads was labelled with an incorrect use before date (ubd) which was greater than the maximum of 36 months shelf life. the date printed on the labels was 5 may 2013 while the correct ubd is 21 september 2012.