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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Philips has become aware that if a footswitch is frequently used on an anti-fatigue mat on a not flat surface or in the pedestal the footswitch pedals may get bent. this might cause an intermittent or continuous inability of making live fluoroscopy images or exposures.