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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In the advia 1200 chemistry system (software versions v2.00 and v2.01) and advia 1650 chemistry system (software versions v3.52 and v4.01) an overflow flag ///// is displayed in the result column for a test when the algorithm for that test cannot calculate a result or when the concentration of a test cannot be determined because it is outside the absorbance limits. ///// is not a usable or reportable result however it is possible for the user to misinterpret or edit this result.