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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Leica microsystems evaluated data showing that a malfunction resulting in an illumination reduction can be observed when leica m525 f50 srugical microscope is used in combination with a remote control connected to a remote video adapter (rva) or a motorized dual video adapter (dva).