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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Unwanted release of evaporating anesthetic agent was observed by users at the end of the filling procedure. the release may lead to spraying of aerosol into face and eyes of the operator. eye contact with volatile anesthetics can result in serious irritation.