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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Cynosure has identified a potential situation where the user of the device could receive an electrical shock under certain conditions. if the laser system is turned on and the user adjusts installs or removes the xpl pulsed light handpiece there is a potential risk of an electrical shock.