FDA MAUDE Adverse Event Reports

View 10000 FDA MAUDE Adverse Event Reports on BEUDAMED, the Better Database on Medical Devices. These entries compile voluntary and mandatory reports of device malfunctions, injuries, and deaths submitted by manufacturers, health care facilities, and users to the FDA's MAUDE system. Searchable fields include device name, event date, reporter type, and narrative descriptions to support safety review and trend detection.

MAUDE reports are a key resource for clinicians, manufacturers, researchers, and regulators monitoring post-market device performance. Users should interpret the data with caution because MAUDE is a passive reporting system subject to incomplete information and potential reporting biases. When combined with clinical judgment and other surveillance sources, these reports help identify signals that may prompt further investigation or corrective action.