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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The biotestcell p3 are reagent red blood cells with polyvalent antigens of three single blood donors packaged in 3 separate vials for the detection of red cell antiobodies. the manufacturer received one complaint about an incorrectly labeled vial within the package. normally the vials come numbered p1 p2 p3. in this case the package contained 1 bottle of p1 and 2 bottles of p2.