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 affected liaison xl label "i" barcode labels may cause an instrument error when being read by the barcode scanner making the rack unusable. control results can be obtained by changing the position of the control in the rack or manual entry of the control information. it is unlikely that patient results would be adversely affected by the liaison xl label "i" barcode labels.