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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Alcon is conducting a voluntary medical device correction of all lx3 microscope floor stands after receiving reports concerning loss of functionality due to issues with the cabling between the power host and illumination modules potentially causing the system to display a system message and/or resulting in illumination failure. alcon will retrofit the cable design on any impacted lx3 microscope floor stands.