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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During an internal review beckman coulter determined that the following global harmonized system hazard classification warnings and european hazard classification warnings for reagent well r1b are missing from the current access stfr instructions for use (ifu) versions.