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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When a sample rack is partially removed after testing is complete and another rack is inserted into an adjacent position it is possible for the partially removed rack to be inadvertantly loaded ahead of the second rack. in this instance the second rack's sample id's will be incorectly assigned to the original rack.