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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When running a multi-tube worklist there is a slight possibility that a listmode file may be duplicated. when this happens the next tube on the worklist is skipped (not sampled). subsequent tubes on the worklist are processed correctly. the duplicated listmode file contains all of the correct data events and fcs keyword information but will have the skipped tube's listmode filename assigned to it. therefore any panel report generated from the skipped tube may have erroneous but credible results.