FDA MAUDE — Medical Device Adverse Event & Malfunction Reports

Search the FDA's **MAUDE database of 24 million+ medical device adverse event reports** — including malfunctions, injuries, and deaths. Filter by device name, manufacturer, product code, event type, report number, or date range.

openFDA Medical Device Adverse Events & Recalls Scraper

scrapers_lat/openfda-device-events-scraper

Scrape FDA medical device adverse events (MAUDE), device recalls and 510(k) clearances from the official openFDA API. Extract report number, device brand, manufacturer, event type, product problems and dates across the United States. Export to JSON, CSV or Excel.

Public data actor with normalized output.

openFDA Medical Device Events Scraper

parseforge/openfda-device-event-scraper

Export MAUDE medical-device adverse-event reports from openFDA. Search 24M+ reports by device name, manufacturer, event type, and event-date range. Pull report ID, device, manufacturer, event narrative, patient outcome, and dates.

Public data actor with normalized output.

FDA Adverse Events Scraper - FAERS + MAUDE Export

maydit/us-fda-adverse-events-scraper

Scrape FDA adverse events from FAERS (drugs) and MAUDE (devices) via openFDA. Deeply nested reports flattened to one clean row each. Export to CSV, JSON, or Excel.

Medtech peer benchmarking intelligence for AI agents. Compare device manufacturers safety profiles against product-code peers using FDA MAUDE, 510(k), and enforcement data.

Fda Intelligence Mcp

ryanclinton/fda-intelligence-mcp

Fda Intelligence Mcp. Available on the Apify Store with pay-per-event pricing.

Query FDA MAUDE adverse events, 510(k) clearances, and device recalls. One tool call for AI agent medical device compliance research.

The FDA's openFDA program contains over 20 million records across drug adverse events, recalls, product labels, medical device malfunction reports, and food enforcement actions. This data drives billion-dollar regulatory decisions — but the raw API is complex, inconsistently...