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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The following allele specificities are missing from the lot specific user documents and catalog file for the labtype hd drb1 typing test (catalog id rssoh2b1 lot 009 batches 1-16): drb1*03:12 drb1*03:16 drb1*04:23 drb1*04:25 drb1*04:32 drb1*04:52 drb1*11:40 drb1*14:142 drb1*15:06:02 drb1*15:74 drb1*15:85 drb3*03:02 drb4*01:05 drb4*01:08 this may cause a mistype for drb1*04:52. a sample with drb1*04:52 would be typed as drb1*04:03:01/03:03/03:05/03:07~03:08 without indicating an ambiguity with drb1*04:52.