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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Olympus is taking corrective action to upgrade the software of esg-400 units after receiving complaints that certain error codes may be generated/displayed during a procedure even though the possible causes for the error codes do not exist. when the error codes are generated high frequency output from the esg-400 generator is suspended and therefore the generation of these incorrect error codees can result in a delay in the medical procedure.