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 method sheet (usrevd) of the inform her2 dual ish dna probe cocktail might have been distributed instead of the version that is provided under the canada folio as indicated on the reagent kit (version enrevb).