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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Jamming of cables in the suspension arm may lead to damage of video and/or related cables caused by an abrasion of the cables located in the suspension arm. there is no risk of harm or safety related to this issue. the opmi lumera 700 can be used in manual mode in the worst case scenario.