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 biosystems richmond inc. has identified a potential error on the cytovision image analysis and capture systems. an issue during the manufacturing process might have caused these systems to have an improperly activated windows 7 operating system even though a valid windows 7 license was associated with each manufactured system. it has been determined these systems cannot be re-activated using standard windows licensing procedures and a check of these systems to confirm windows is properly activated is required.