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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If an unrecognized rack is removed and a sample is than removed or switched in the rack followed by reinserting the rack into the lane it is possible for the sample id that originally occupied the possition to be assigned to the newly loaded sample or the the empty position. under these conditions it is possible that results will be associated with the wrong sample.