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
physiological patient monitor - Product Code MHX
원인
Intermittent or continuous loss of patient monitoring.
조치
Consignees were sent on 2/20/09 a GE Healthcare "Urgent Medical Device Correction" letter dated 2/12/09. The letter was addressed to Risk Manger/Chief of Nursing/Director of Biomedical Engineering. The letter described the Safety Issue, Affected Product Details, Safety Instructions, Product Correction and Contact Information.