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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L'utilisation du profil phenotypique inclus dans le coffret dans l'evaluation des reactions positives aurait produit des resultats discordants ou ambigus. il existe une possibilite de mal identifier les anticorps anti-jk(b) et -s et des problemes transfusionnels que cela aurait pu causer.