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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Immulite/immulite 1000 total t3 reagent wedge bar code for kit lot 349 is not reading appropriately to correspond to the kit bar code. a number of bar codes from manufacturing run of lt32 1098 have been found to read as lot zero.