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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One customer complaint was received (pr# 125459). a sample representing dpb1*61:01n is incorrectly designated as positive in lanes 19 27 and 30. customers who may test a sample with this allele would obtain a no type test result.