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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Keeler ltd has recently updated the cryomatic probe user instruction kcu 402 from issue 1 to issue 2 regarding the sterilization methods to be used. a technical bulletin had been supplied to all users describing the changes. it has now been discovered that issue 1 of the instruction has been supplied with probes distributed between the 1st of september 2010 and the 26th of april 2011.