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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In certain limited instances particularly when the unit is rebooted the system may project through the slit lamp's oculars an erroneous display which is different than the desired pattern. although an unlikely occurrence this represents a potential safety matter. in these rare cases if the heads-up display does not match the desired pattern promptly discontinue the treatment and restart the system.