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 cobas liat system allows the use of several different barcode types for sample identification. if any of these barcode types are used together with codabar or code 39 barcodes and match an existing codabar or code 39 exactly it is theoretically possible that a sample mismatch between the two samples could occur when using software version 3.0.