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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We have received reports of instances where the snare loop has separated from the shaft of the device. the issue appears to be related to/caused when lateral forces are applied to the loop/shaft connection (e.G. in three reports separation occurred after attempts by a user to reshape the tip of the device). the issue was uncovered during a customer complaint investigation.