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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Qfc1716int is an accessory to the system 1 express sterile processing system. this quick connect consists of labeling and a flow unit made up of tubing tethers and adapters used for connecting ports of specified fujinon devices to flexible processing trays/containers placed within the system 1 express. steris has learned that the suction connector barb adapter on the qfc1716int does not properly fit the suction connector port of the fujinon 530 series endoscopes and consequently disconnects from the endoscope prior to reprocessing.