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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Ortho clinical diagnostics (ocd) has received a report that when using a hand-held barcode scanner in combination with use of the batch programming option for programming samples the scanner unexpectedly skips sample cup positions. for example a sample tube barcode is scanned for the cup 1 position the cursor in the batch programming screen skips the cup 2 position and advances to the cup 3 position. if this anomaly occurs there is a potential for mis-associated results.