Retiro De Equipo (Recall) de Digital diagnostic x-ray equipment, Digital diagnostic x-ray equipment, Digital diagnostic x-ray equipment

Korean data is current through September 2018. All of the data comes from Korean Food & Drug Administration, 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 South Korea.

Su-in 03-780, Su-in 07-729, Su-in 07-730