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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Biotest cell 1 et 2 contiennent des hematies de phenotypes connus servant au depistage des anticorps lors des epreuves serologiques en immunohematologie. dans un avis transmis le 11 septembre bio-rad medical diagnostics gmbh ont rapporte que les hematies du lot 8731011-00 contenues dans le flacon 1 (donneur no. 100136) ont ete declarees comme etant du phenotype fy(a+ b-) alors que le phenotype correct est fy(a+ b+ w).