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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Fujifilm has become aware of events in which the suction button on the ed-530xt endoscope may become lodged (stuck) in the active position following the use of x-ray contrast agents during ercp procedures. the contrast agent gets sticky and can solidify upon drying causing the suction button to become lodged.