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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Through alcon's monitoring process alcon has observed that multiple shipments or forceful impact to a caster on a luxor/lx3 microscope may stress the microscope base which could contribute to a caster breaking or detaching from the base. this may lead to the potential for physical injury from the microscope tipping or falling.