U.S. data is current through June 2018. All of the data comes from the U.S. Food and Drug Administration, except for the category Manufacturer Parent Company.
The Parent Company was added by ICIJ.
The parent company information is based on 2017 public records.
데이터 추가 비고
Digital Radiographic System - Product Code KPR
원인
Radiation dose reading greater than actual dose: error in the generator software on the ge healthcare revolution xr/d configured with hp 8200 pc consoles and all definium 8000 systems may impact patient safety. occasional generator software errors may cause light x-ray images with reported mas readings higher than was actually exposed to the patient using the overhead x-ray tube. the mas rea.
조치
GE sent a Product Safety Notification dated March 7, 2008 to all customers. The letter described the safety issue, affected product, and stated that a GE Healthcare Field Engineer will schedule a field visit to install software updates.