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 auto stop and auto transmit features for quality control become disabled after scanning assay values from coulter 5c and retic-c cell controls assay sheets using the 2d barcode scanner.