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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Caridianbct has become aware of a small number of cases where patients have experienced higher than expected platelet loss following therapeutic plasma exchange (tpe) or plasmapheresis conducted using caridianbct's spectra optia apheresis system.