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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3m received a single report of a potential exposure ot ethylene oxide (eo) at a hospital installation outside of canada. the cause was traced to a rare situation involving a failure of the eo cartridge puncture assembly part manufactured between november 10 2006 and december 14 2007.