FDA Investigating Reports of Infections Associated with Reprocessed Urological Endoscopes
Endoscopy Insights PodcastThe FDA is investigating “numerous” medical device reports (MDRs) describing patient infections and other possible contamination issues possibly associated with reprocessed urological endoscopes. Dr. Larry Muscarella talks about the letter to healthcare providers from the FDA.
The FDA’s Safety Communication Update for Reprocessing Bronchoscopes
Endoscopy Insights PodcastThe U.S. Food and Drug Administration recently updated a safety communication on reprocessing flexible bronchoscopes. To break down this announcement and what it means, we talked to Dr. Hudson Garrett, an infection prevention and control expert.