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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Siemens has confirmed a negative bias against the mean values obtained with the lgcocm control lot 0026 level 2 when used with immulite/immulite 1000 igf-1 (lkgf1) kit lots 322 and above. also confirmed is an increase of mean values obtained with the lgcocm control lots 0025 025l & 0026 when used with immulite 2000/immulite 2000 xpi igf-1 (l2kgf2) kit lots 486 and 487.