FDA Medical Device Adverse Event Search (MAUDE)

FDA Medical Device Recall Search queries the U.S. Food and Drug Administration's openFDA device enforcement endpoint to retrieve detailed, structured data about medical device recalls.

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

openFDA Drug & Device Data Crawler

jungle_synthesizer/openfda-drug-crawler

Crawl FDA drug adverse events, recalls, labels, NDC codes, device events, and 510(k) clearances from the openFDA API. Filter by drug name, manufacturer, date range, and severity. 20M+ adverse event reports available.

Public data actor with normalized output.

Search the FDA's **CAERS database of 148,000+ adverse event reports** for foods, dietary supplements, and cosmetics. Find reports by product name, reaction/symptom, industry type, outcome severity, consumer demographics, or date range.

Search the FDA's database of **174,000+ 510(k) premarket notification clearances** for medical devices. Filter by device name, company, product code, advisory committee, decision type, clearance type, date range, or country.

FDA 510(k) Device Clearance Monitor

pink_comic/fda-510k-medical-device-clearances

Monitor new FDA 510(k) medical device clearances daily. Schedule runs to track clearances by device type, applicant, or product code. For medtech companies, investors, regulatory consultants, and competitive intelligence. Pay per result.

Search FDA databases for drug labels, adverse events, recalls, and medical devices. Essential for pharmaceutical and healthcare research.

The openFDA Drug Event Monitor searches the FDA Adverse Event Reporting System (FAERS) database, which contains millions of reports of adverse drug reactions submitted to the U.S. Food and Drug Administration.

FDA Recalls Scraper

automation-lab/fda-recalls-scraper

Search FDA enforcement database for drug, food, and medical device recalls. Get recall classifications, reasons, product descriptions, and distribution data.