Japanese data is current through August 2018. All of the data comes from the Japanese Pharmaceuticals and Medical Devices Agency, 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 Japan.
데이터 추가 비고
2016/12/19 "2. Target Lot, Quantity and Shipment Timing", "6. Correction of Start Date of Collection", "9. Correction of Person in Contact and Contact" 2017/8/2 "9. Person in charge and contact Correction to "2." 2018/3/5 "2. Target Lot, Quantity and Shipment Timing" "9. Personnel and Contact Information" 2018/4/13 Correction and Recovery of "2. Target Lot, Quantity and Shipment Timing" End