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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A software error in the juan/thermo-fisher c4i centrifuge sold with the prepstain system causes the centrifuge to display an inaccurate g force or rpm reading during operation. in each case that has been investigated the centrifuge was operating properly but the display was showing a value that was lower than the true value.