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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Beckman coulter inc. identified a problem with the barcode labels for the lin-x (lot numbers 2681530k 2661580k). the unicel dxht 800 coulter cellular analysis system generated the error message 'xml parsing error' when attempting to read the label for any lin-x level prior to analysis. an additional character that was included in the label caused the error.