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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Under certain circumstances results could be assigned to a wrong sample. when the operator registers an order for micro mode and tries to modify the order by pushing the button in the order screen or the job list screen there is a risk of a mismatch between results and sample id numbers. the problem concerns qc as well as sample measurements which are measured in normal-mode. please note that this problem occurs even if no modification of the sample order has been done. pushing the button already triggers the error which is caused by a possible wrong feed forward of the sample rack.