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.
데이터 추가 비고
원인
The macro component intended to be used with the factor ii g20210a kit for light cycler 2.0 instrument may erroneously identify the c20209t mutation as a wild-type genotype instead of an unknown genotype.