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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Higher than normal number of false negative tests for anti-fya. product lots involved showed reduced potency with respect to the detection of antibodies to the fya human red cell antigen. see 019978.
Model Catalog: (Lot serial: DEV LIC # 1079); Model Catalog: (Lot serial: 07622 09671); Model Catalog: (Lot serial: TEST KITS 05558 07616); Model Catalog: (Lot serial: ID48 ID49)