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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This recall has been initated due to potential loss of data when an anti-virus program scans eye station (es) or eye care pacs (ecp). during a scan the anti-virus program may detect a newly captured image to be an unwated file and delete the image permanently.