FDA MAUDE Adverse Event Reports Scraper

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.

FDA MAUDE Device Event Monitor

technicaldost/fda-maude-device-events-monitor

Monitor medical device adverse events from openFDA MAUDE data.

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.

US FDA Adverse Events Scraper (FAERS + MAUDE)

maydit/us-fda-adverse-events-scraper

Search FDA adverse-event reports for drugs (FAERS) and medical devices (MAUDE) as clean, flattened records.

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.

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

Signal-scored adverse-event feed from openFDA FAERS (drugs) + MAUDE (devices). Returns reports with seriousness flags, MedDRA Preferred Terms, and PRR disproportionality signal per drug-event pair. For pharmacovigilance, mass-tort plaintiff intake, device compliance, medical journalism.

FDA Food Adverse Events Scraper

crawlerbros/fda-food-adverse-events-scraper

Scrape the FDA CFSAN Adverse Event Reporting System (CAERS) - search 140,000+ food, dietary supplement, and cosmetic adverse event reports by product, reaction type, or date range. No API key required.

Public data actor with normalized output.

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