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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It has been determined that the threshold set for hla-c eres probes 380 382 384 and 385 are set high and may result in false negative probe results. the probes resolve the following cwd alleles probe 380 resolves c*03:06 probe 382 resolves c*12:13 probe 384 resolves c*01:08 and probe 385 resolves c*08:06.