Pricing

from $5.50 / 1,000 event searches

Try for free

Go to Apify Store

FDA MAUDE Search: Medical Device Adverse Events

Try for free

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.

Pricing

from $5.50 / 1,000 event searches

Rating

0.0

(0)

Developer

Timothy Kelvin

Actor stats

Bookmarked

Total users

Monthly active users

11 days ago

Last modified

Medical Device Adverse Event Tracker — FDA MAUDE Reports

Search FDA MAUDE (Manufacturer and User Facility Device Experience) adverse event reports by device name and event type. These are raw incident reports — malfunctions, injuries, deaths associated with a device — not official recalls, and often the earliest public signal of a device problem.

Built for hospital risk management, device safety teams, and researchers who want to know what's being reported before it becomes an official recall.

Input

{
  "deviceName": "insulin pump",
  "eventType": "all",
  "daysBack": 30,
  "maxResults": 25
}

Field	Type	Description
`deviceName`	string (optional)	Free-text search across the device's generic name.
`eventType`	string	`"all"`, `"Malfunction"`, `"Injury"`, or `"Death"`. Default `"all"`.
`daysBack`	number	How many days back from today to search, by date received by FDA. Default `30`, max `365`.
`maxResults`	number	Max reports to return, most recently received first. Default `25`, max `100`.

Output

One record per report:

{
  "reportNumber": "2124215-2026-35065",
  "eventType": "Injury",
  "dateReceived": "2026-07-01",
  "dateOfEvent": "2026-06-19",
  "deviceGenericName": "PACEMAKER",
  "deviceBrandName": null,
  "manufacturer": "MEDTRONIC",
  "productProblemFlag": true,
  "reporterOccupation": "PHYSICIAN"
}

A search with no matching reports returns no items but is still billed once for the search.

How it works

Direct calls to the official openFDA Device Adverse Event API (api.fda.gov) — no proxy, no key, no scraping.

Note: these are unverified reports submitted by manufacturers, health professionals, and consumers — FDA publishes them as filed, without confirming a device caused the reported outcome. Treat volume and pattern as a signal worth investigating, not proof of a defect.

Pricing note

Billed per search, not per report returned — one charge whether the search returns 0 reports or 100.

FDA Recall Tracker: official FDA drug, food, and device recalls, the confirmed-issue counterpart to this actor's raw incident reports
Vehicle Complaint Lookup: the same raw-complaints-before-recall pattern for vehicles instead of medical devices

EUDAMED Medical Device Companies Scraper

scrapers_lat/eudamed-medical-device-actors-scraper

Directory of EU EUDAMED-registered medical device operators: manufacturers, authorised reps, importers and pack producers with email, phone, EU VAT, EORI, trade register number and named regulatory-compliance contacts. JSON, CSV, Excel.

Scrapers Lat

🇪🇺 EU Medical Devices (EUDAMED) — Device & Manufacturer Data

inexhaustible_glass/eu-medical-devices

Scrape EU-registered medical devices from EUDAMED (2.6M+). Device, risk class, status, manufacturer & EU authorised representative. MDR/IVDR compliance & medtech leads. Free, no key, no proxy.

Hitman studio

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 510(k) Scraper - Medical Device Clearance API

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

Search FDA 510(k) medical device clearances via the official OpenFDA API. Use this scraper/API to find cleared devices by name, applicant, product code, or decision date and monitor competitor approvals, regulatory decisions, and predicate devices. No FDA API key needed.

Ava Torres

openFDA Device Adverse Events Scraper

neuton/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.

Neuton Scripts

openFDA Food Adverse Events Scraper

neuton/openfda-food-adverse-events-scraper

Extract FDA CAERS food adverse event reports from openFDA for product safety monitoring, supplement research, and consumer-health risk analysis.

Neuton Scripts

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 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

Medical Device Records — FDA 510(k) & PMA API

nexgendata/medical-device-fda-intelligence

Track FDA medical device 510(k) clearances and recalls from official openFDA data: applicant, device, product code, class, decision date, and Class I/II/III recall severity. For medtech intelligence.

NexGenData

FDA Adverse Events — FAERS & MAUDE Records API

nexgendata/fda-adverse-events-faers-maude

Adverse-event feed from openFDA FAERS (drugs) + MAUDE (devices): source-linked reports with seriousness flags, MedDRA Preferred Terms, and a PRR screening score over the reports each run retrieves (sample-level, not a population signal). Pharmacovigilance, mass-tort intake, device compliance.

NexGenData