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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Conmed received five complaints of some devices which had broken through the seal of the sterile pouch: the initial complaint was received on november 30 2012. conmed has confirmed instances where the pouch seal was compromised on the affected products. in no instance has it been reported to conmed corporation that a compromise in the sterile barrier has resulted in illness or injury. the compromised seals were discovered prior to use.