Pricing

$3.00 / 1,000 results

openFDA Device Adverse Events Scraper

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

Pricing

$3.00 / 1,000 results

Rating

0.0

(0)

Developer

Ashwin Prasad

Actor stats

Bookmarked

Total users

Monthly active users

3 days ago

Last modified

What it returns

MDR report key and report number
Event type, event date, and received date
Manufacturer, device name, product code, patient outcome
Event description and manufacturer narrative when published
Official MAUDE detail URL and raw openFDA record

The actor supports optional openFDA API keys for higher production rate limits, but small runs work without a key.

Common use cases

Monitor medical device adverse event reports for safety surveillance
Track manufacturer, device, product code, and patient outcome patterns
Support regulatory intelligence, complaint trend analysis, and post-market monitoring
Enrich health-tech compliance dashboards, RAG systems, and analyst workflows
Build competitor and product-risk datasets from official MAUDE/openFDA records

Agent and automation workflows

Use this actor as an official MAUDE/openFDA data connector for Apify schedules, webhooks, BI dashboards, health-tech compliance monitors, and AI agents. Agents can watch a device name, manufacturer, or product code, summarize new event narratives, and send structured rows into internal safety-review queues.

Sample input

{
  "searchTerms": [
    "x-ray"
  ],
  "maxResultsPerSearch": 5
}

SEO keywords

openFDA device adverse events scraper, MAUDE adverse event API, medical device safety data, FDA device event reports, medical device complaint monitoring, device manufacturer intelligence, product code adverse events.

Pricing recommendation

Launch around $3 per 1,000 adverse-event rows. Increase toward $5 per 1,000 rows after recurring health-tech, regulatory, or product-safety monitoring usage appears.

Responsible use

This actor uses public FDA/openFDA records. It is intended for monitoring and research, not medical advice; validate critical safety decisions against the official FDA source and qualified reviewers.

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.

ParseForge

FDA MAUDE — Medical Device Adverse Event & Malfunction Reports

samwise.agency/fda-device-maude

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.

samwise.agency

FDA MAUDE Device Event Monitor

technicaldost/fda-maude-device-events-monitor

Monitor medical device adverse events from openFDA MAUDE data.

Technical Dost Solutions

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.

Scrapers Lat

5.0

FDA MAUDE Medical Device Adverse Events Scraper API

pink_comic/fda-maude-device-events

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.

Ava Torres

FDA Medical Device Adverse Event Search (MAUDE)

ryanclinton/fda-device-events

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.

Ryan Clinton

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.

Scrape Sage

Healthcare Compliance MCP — AI Agent FDA Device Intelligence

red.cars/healthcare-compliance-mcp

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

AutomateLab

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.

BowTiedRaccoon

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.

Ryan Clinton