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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When tested in conjunction with bd probetec ct/gc positive control returned strips from full and partially used ct microwell pairs from the indicated bd probetec ct/gc/ac reagent pack batches yield invalid ct positive control results.