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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Misassembled lcrd2 and mtl1 filters were reported to macopharma where the inlet and the outlet tubing were on the same side of the filter. this misassembly creates direct passage of blood from the collection bag to the transfer bag without passing through the filter.