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
Lane 23 in the 'a' high resolution ssp unitray lot and batch number identified will produce a false positive band at the correct base pair size in the presence of a*0301 samples. this will affect typing results on samples that are a*0301 homozygote since they could be erroneously reported as a*0301/a*1101.