Class We recall for Vital Signals HCH/Anesthesia Breathing Circuit In April 2011.
All affected Hygroscopic Condenser Humidifier and Anesthesia Breathing Circuits with affected Hygroscopic Condenser Humidifiers are becoming replaced. The U.S. Food and Drug Administration has categorized this recall as a Course I recall. FDA defines Class I recalls as ‘a situation in which there is a reasonable probability that the use of or exposure to the volatile product may cause serious adverse health consequences or death.’.. Class We recall for Vital Signals HCH/Anesthesia Breathing Circuit In April 2011, Vital Signs Devices, a GE Healthcare Company, initiated a voluntary worldwide field correction of the Essential Signs Hygroscopic Condenser Humidifier /Anesthesia Breathing Circuit.Patients in the analysis were enrolled in the Shanghai Breast Cancers Survivor Study, a large, population-based overview of female breast malignancy survivors in China, which Vanderbilt University INFIRMARY and the Shanghai Institute of Preventive Medicine have completed since 2002 beneath the leadership of principal investigator Xiao Ou Shu, M.D., Ph.D., professor of Medicine at VICC, and senior author of the study. From 2002 to 2004, a total of 2,230 breast cancer survivors completed an excellent of life survey six months after diagnosis and a majority responded to a follow-up survey 36 months after diagnosis.