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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Immucor has received reports that plates of capture-r ready-id (lot id 296) are being aborted due to "measurement out of range" errors after the strip clean read on the galileo neo instrument due to cell 13 exhibiting a yellow color.