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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Beckman coulter has identified an increase in customer complaints reporting waste leaks from the volume conductivity scatter (multi-channel) (vcsn) waste chambers (vc222) and complete blood count waste chambers (vc115) on the unicel dxh 800 coulter cellular analysis system and the unicel dxh 600 coulter cellular analysis system analyzers.