Multi-use Website Reprocessing of Reusable Medical Devices. Citation Text: Reprocessing of Reusable Medical Devices. US Food and Drug Administration. Copy Citation Save Save to your library Print Download PDF Share Facebook Twitter Linkedin Copy URL September 22, 2015 US Food and Drug Administration. This Web site provides resources to help ensure safe reuse of medical devices. Available at Related information (PDF) Save Save to your library Print Download PDF Share Facebook Twitter Linkedin Copy URL Cite Citation Citation Text: Reprocessing of Reusable Medical Devices. US Food and Drug Administration. Copy Citation Related Resources From the Same Author(s) FDA alerts patients and health care professionals of EpiPen auto-injector errors related to device malfunctions and user administration. April 8, 2020 Medication errors resulting from confusion between risperidone (Risperdal) and ropinirole (Requip). June 22, 2011 Wear face masks with no metal during MRI exams. December 16, 2020 Initiative to Reduce Unnecessary Radiation Exposure from Medical Imaging. July 31, 2012 Infections associated with reprocessed flexible bronchoscopes. September 30, 2015 FDA requires label warnings to prohibit sharing of multi-dose diabetes pen devices among patients. March 11, 2015 Design of endoscopic retrograde cholangiopancreatography (ERCP) duodenoscopes may impede effective cleaning. March 4, 2015 FDA Drug Safety Communication: FDA cautions about dosing errors when switching between different oral formulations of antifungal Noxafil (posaconazole); label changes approved. January 13, 2016 Differences in strength expression on product labels of compounders and conventional manufacturers may lead to dosing errors. October 10, 2018 Be an Active Member of Your Health Care Team. May 21, 2014 View More Related Resources FDA identifies harm reported from sudden discontinuation of opioid pain medicines and requires label changes to guide prescribers on gradual, individualized tapering. April 17, 2019 NHS Resolution. March 7, 2018 BeSafeRx: Know Your Online Pharmacy. January 25, 2018 RxAwareness. October 25, 2017 Indiana Patient Safety Center. August 17, 2016 Questions Are the Answer. March 22, 2016 Healthcare–Associated Infections (HAI). May 20, 2015 Medication Safety Program. June 11, 2014 Promethazine HCl (marketed as Phenergan) Information. June 23, 2009 Postmarket Drug Safety Information for Patients and Providers. November 19, 2008 View More See More About The Topic Health Care Providers Patients Medicine Practice Guidelines Online Education
FDA alerts patients and health care professionals of EpiPen auto-injector errors related to device malfunctions and user administration. April 8, 2020
Medication errors resulting from confusion between risperidone (Risperdal) and ropinirole (Requip). June 22, 2011
FDA requires label warnings to prohibit sharing of multi-dose diabetes pen devices among patients. March 11, 2015
Design of endoscopic retrograde cholangiopancreatography (ERCP) duodenoscopes may impede effective cleaning. March 4, 2015
FDA Drug Safety Communication: FDA cautions about dosing errors when switching between different oral formulations of antifungal Noxafil (posaconazole); label changes approved. January 13, 2016
Differences in strength expression on product labels of compounders and conventional manufacturers may lead to dosing errors. October 10, 2018
FDA identifies harm reported from sudden discontinuation of opioid pain medicines and requires label changes to guide prescribers on gradual, individualized tapering. April 17, 2019