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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Avec le niveau 2 du produit quantify control lot 78512 on rapporte des valeurs negatives pour les leucocytes sur les bandelettes utilisees avec les appareils bayer clinitek 100 et 500.