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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Quick connects provide directed flow of processing fluids (sterilant use dilution and rinse water) into the internal lumens of specifically identified endoscopes via adapters which connect to the endoscope ports. each quick connect contains a flow unit consisting of tubing tethers and adapters for connecting the medical device to the system 1 express processing tray to achieve liquid chemical sterilization. steris has learned that one of the hysteroscope models (karl storz 11264bbu1) listed for processing in two existing quick connects has one inlet port rather than two inlet ports as indicated in the quick connect processing instructions. a user who connects the karl storz 11264bbu1 hysteroscope according to the processing instructions will observe an unused port adapter on the quick connect.