openFDA Medical Device Events Scraper

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.

Search FDA MAUDE medical device adverse event records through openFDA. Export report numbers, event types, dates, manufacturers, device names, patient outcomes, and narrative text.

Search FDA MAUDE (Manufacturer and User Facility Device Experience) adverse event reports for medical devices. Report numbers, device names, manufacturer names, event types, dates, patient outcomes, and product problems. Official openFDA data, no API key.

FDA MAUDE Device Event Monitor

technicaldost/fda-maude-device-events-monitor

Monitor medical device adverse events from openFDA MAUDE data.

Search FDA MAUDE adverse event reports for medical devices by device name and event type (malfunction, injury, death). Raw incident reports, not official recalls, for device safety monitoring.

Search FDA MAUDE adverse-event reports by report, manufacturer, device, product code, event, dates, patient outcome, and device problem. Returns source-linked nested device and patient evidence with mandatory non-causation limits.

FDA Medical Device Recall Search

ryanclinton/fda-device-recalls

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.

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.

FDA Scraper - Recalls, Adverse Events & Device Data

scrapesage/fda-scraper

Scrape the U.S. FDA (openFDA): drug, device & food recalls, adverse events (FAERS/MAUDE/CAERS), 510(k) & PMA device clearances, drug labels/approvals/NDC, and medical-device manufacturer leads. Keyless, no browser, monitor mode + analytics.

Extract FDA medical device UDI records for device identification, product-code enrichment, manufacturer intelligence, and compliance workflows.