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 bindazyme human c1q binding circulating immune complex eia kit may contain an elisa plate labeled as 'tissue transglutaminase coated wells" instead of c1q coated wells.