Two-thirds of U.S. recalls start as an adverse event report. Reporting side effects linked to medical devices, implants or medications is the single most important data source driving recalls. You can help save lives by reporting your side effects to the FDA.

Watch our 4-minute video on the importance of adverse event reporting.

Hear from industry experts and patient advocates about the importance of reporting adverse events to the FDA.

The PSA film features, in order of appearance:

Maria Gmitro, President of the Breast Implant Safety Alliance

Madris Tomes, CEO & Founder of Device Events

Dr. Rita Redberg, cardiologist at UCSF Health and editor of JAMA Internal Medicine

Robert Cartwright, Founder and Managing Partner of the Cartwright Law Firm

Jeremy Elias, CEO & Founder of TrackMy

Get a step-by-step guide on how to report an adverse event to the FDA.