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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Cisbio bioassays rapporte avoir identifie un defaut dans l'emballage de la trousse igf1-ria ct lot 205a. certaines trousses contiendraient 1 ou 2 fioles de la trousse cal0 aldo-ria ct lot 22a au lieu des fioles buf igf1-riact lot 22a.