1. 5. FDA recommends healthcare facilities and manufacturers begin transitioning to duodenoscopes with disposable components to reduce risk of patient infection. US Food and Drug Administration webiste. https://www.fda.gov/news-events/press-announcements/fda-recommends-health-care-facilities-and-manufacturers-begin-transitioning-duodenoscopes-disposable. Published 2019. Accessed January 3, 2023.
2. 2. Preventable tragedies: superbugs and how ineffective monitoring of medical device safety fails patients. US Senate Committee on Health, Education, Labor, and Pensions website. https://www.help.senate.gov/ranking/newsroom/press/preventable-tragedies-superbugs-and-how-ineffective-monitoring-of-medical-device-safety-fails-patients. Published January 13, 2016. Accessed January 3, 2023.
3. 3. Design of Endoscopic Retrograde Cholangiopancreatography (ERCP) duodenoscopes may impede effective cleaning: FDA safety communication. US Food and Drug Administration webiste. http://www.fda.gov/MedicalDevices/Safety/AlertsandNotices/ucm434871.htm. Published 2015. Accessed March 31, 2015.
4. 4. Infections associated with reprocessed duodenoscopes. US Food and Drug Administration website. http://www.fda.gov/MedicalDevices/ProductsandMedicalProcedures/ReprocessingofReusableMedicalDevices/ucm454630.htm. Published 2016. Accessed January 5, 2017.
5. Prospective assessment of the effectiveness of standard high-level disinfection for echoendoscopes