OpenFDA Search Device Adverse Events

Search the FDA MAUDE medical-device adverse-event database via openFDA. Contains voluntary and mandatory reports of device-associated injuries, malfunctions, and deaths. Returns event type (Death/Injury/Malfunction), device brand/generic name, manufacturer, product problems, patient outcomes, and report dates. Use for device safety signal detection and post-market surveillance. MAUDE reports are unverified and do not establish causation.