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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This correction alerts the customers to a software problem that causes possible false low wbc counts when using the low wbc mode. three other software anomalies related to abnormal sample flagging were also identified in this software version.