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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Sciex is initiating a field action for the multiquant md software versions 3.0 3.0.1 and 3.0.2. multiquant md software is for use with the api 3200md lc/ms/ms system 3200md qtrap lc/ms/ms system triple quad 4500md lc/ms/ms system and qtrap lc/ms/ms system. an issue has been identified with multiquant md software where under certain conditions a user can be presented with incorrect quantitative results when using the sum multiple ions feature.