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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Lane 27 (r04-28a) in the drb1*04 ssp unitray kit lots and batches mentioned was found to produce a false positive band in the correct base pair size. this will affect typing results on samples that are drb1*0401 homozygotes since they could be erroneously reported as drb1*0426.