Do you know that hospital acquired infections (HAIs) can have a direct correlation to reprocessed medical devices according to a Johns Hopkins study published in October 2018?1 Have you read that The ECRI Institute, an independent and trusted authority on healthcare practices and products that improve the safety, quality, and cost-effectiveness of patient care, listed “Mishandling Flexible Endoscopes after Disinfection Can Lead to Patient Infections” with an emphasis on reprocessing on the “2019 Top 10 Health Technology Hazards”?2
Does your facility reprocess single-use medical devices (SUDs)? Did you know that reprocessing SUDs can carry risks and disadvantages?
Healthcare facilities are becoming more concerned about reprocessing SUDs (devices intended for one use or use on a single patient during a single procedure). Studies have found a significant rate of physical defects, performance issues, or improper decontamination associated with reprocessing of SUDs. According to the American Congress of Obstetrics and Gynecology, “The use of a reprocessed single-use device provides no direct benefit to an individual patient or her physician.”1