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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Terumo bct records indicate you have received the above catalog number and product lots. the affected trima accel disposable sets catalog number 82408 were mislabeled as trima accel lrs platelet + 35 ml sampler multiplasma rbc sets despite having been manufactured with a 10 ml bacterial sampler.