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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There is a potential defect in the ceiling sa suspension arms of the maquet surgical lights model powerled hled xten standop volista and hanaulux. maquet received some complaints of grinding on double or triple arm suspensions with paint possibly chipping from the junction between two arms. paint chips or particles can fall down from the suspension. this may happen during surgical procedures and paint chips may fall inside the surgical field of a patient.