Discussions in Infection Control

An independent site by Lawrence F Muscarella PhD -- a national authority on the causes and prevention of healthcare-associated infections and related errors.

Tag: AdhesiveDeterioration

Adverse Event Reports Bronchoscopes Colonoscopes Cystoscopes Duodenoscopes ENT Endoscopes Flexible "ENT" Laryngoscopes Food and Drug Administration Gastroscopes GI Endoscopes MAUDE Medical Device Reports (MDRs) Olympus GF-UCT180 Pentax ED-3490TK Single-Use Disposable Devices Urological Endoscopes

Contamination of Flexible Endoscopes and Associated Infections A Comprehensive Review and Analysis of FDA Adverse Event Reports

January 28, 2022 Lawrence F Muscarella PhD

This review analyzed more than 10,000 medical device reports submitted to FDA since 2014 describing the contamination of a flexible endoscope.

You missed

Aseptic Technique Immediate Use Steam Sterilization (IUSS) Joint Commission (JCAHO) Multisociety Guidance Position Statement

Immediate Use Steam Sterilization for Surgical Instruments: Dr. Muscarella’s Guidance and Position Statement

November 26, 2025 Lawrence F Muscarella PhD
Gastroenterology & Endoscopy News Immediate Use Steam Sterilization (IUSS) Instrument Reprocessing Joint Commission (JCAHO) Monitoring Rinse Water Multisociety Guidance Rigid Laryngoscopes Sheaths Spaulding's Device Classification

Dr. Muscarella’s Review of the New Multisociety Guidance for Disinfection and Sterilization in Healthcare Facilities

November 11, 2025 Lawrence F Muscarella PhD
Centers for Medicare and Medicaid Services (CMS) Endoscope-Associated Infections Healthcare Quality, Safety Healthcare-Acquired Infections Medicare's HAC Reduction Program

A Proposal to Include ‘Endoscope-Associated Infections’ as a Reportable Medicare Measure to Promote Patient Safety

July 28, 2025 Lawrence F Muscarella PhD
Adverse Event Reports Food and Drug Administration Food Drug and Cosmetic Act Informed Consent Medical Device Reports (MDRs) Misbranded Devices Patient Notification Warning letters (FDA)

Hundreds of Thousands of Device Reports Were Submitted Late to FDA, a New Study Has Found, Raising Safety Questions

May 13, 2025 Lawrence F Muscarella PhD