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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An issue has been confirmed with the acute care testpak calpak and dilpak barcode labels not scanning on the stratus cs systems. only stratus cs systems with serial numbers 98050001 thru 98052309 are affected. issues were observed with myoglobin ddmr ctni and pbnp. when these errors occur patient results cannot be generated.