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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Ondal acrobat 2000 spring arms manufactured between 2000 and 2006 and used in some helion and xenion surgical light systems may develop metal fatigue fractures over time on the front of the spring arm. arms holding non-camera ready light heads and flat panels are affected too.