FDA device adverse events

Summarize FDA medical device adverse event reports (openFDA MAUDE) for a device name, brand, product code or manufacturer: total matching reports, counts by event type (death, injury, malfunction), the most reported device problems, and the newest reports with date, event type, device, manufacturer, problems and a short excerpt of the event description. Counts cover every matching report; the report list is a capped sample and says so. Optional since date. Live FDA data, no key.