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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Women who undergo both essure procedure and an endometrial ablation may be at increased risk for certain events known to be associated with each procedure. bayer has chosen to notify consignees of the information.