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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During a colonoscopy patient experienced a perforation of the colon. surgery was performed. after the colonoscopy the devices were flushed as per normal routine. during the after-use process it was observed that the co2 flow through the colonoscope couldn't be stopped by the co2 valve of-b194. patient subsequently passed away.