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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During servicing a user error occurred that caused a surgical headlight to be drawn into the magnet causing damage to the light & could potentially cause injury to hospital personnel and/or patients. no hospital staff or patients were involved in this incident.