230,000 Medical Device Adverse Events Reported to FDA in 2010

Of the more than 230,000 medical device-related adverse events reported to the Food and Drug Administration in 2010, approximately 30,000 yielded “very serious” outcomes such as hospitalization or death, according to research conducted by Clarimed.

Advertisement
By: Staff

Read the full report in Becker’s ASC Review on medical device-related adverse events.

At the Becker's 11th Annual IT + Revenue Cycle Conference: The Future of AI & Digital Health, taking place September 14–17 in Chicago, healthcare executives and digital leaders from across the country will come together to explore how AI, interoperability, cybersecurity, and revenue cycle innovation are transforming care delivery, strengthening financial performance, and driving the next era of digital health. Apply for complimentary registration now.

Hiring Under Pressure: How Healthcare Organizations Can Scale Recruiting While Reducing Fraud Risk

Recommended Live Webinar on Jun 2, 2026 1:00 PM - 2:00 PM CDT

Advertisement

Next Up in Clinical Leadership & Infection Control

Advertisement

Comments are closed.