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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Ge healthcare has become aware of a potential issue associated with the hand grip that is clamped to the table top of your revolution xr/d x-ray systems that may impact patient safety. the hand grip accessory that is clamped to the table top may not be properly adjusted and can dislodge during use. should this happen during patient loading or unloading patient injury could occur.