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 has received complaints of damage to the cs-203 electrode's shaft insultation which could result in burn marks on the shaft. if the shaft insulation is damaged in anyway it could increase the risk of patient burn.