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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The unicel dxh 800 coulter cellular analysis system with revision 2.0.0.1 software transmits the white blood count (wbc) red blood count (rbc) and platelet (plt) histograms with an incorrect identifier to the host causing the host to not be able to retrieve the data. all languages are impacted by this issue.