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openfda_devices.adverse_events

mock data$0.002 / call

FDA Medical Device Adverse Events (MAUDE)

Search FDA MAUDE database for medical device adverse event reports — 25M+ records of device malfunctions, injuries, and deaths. Returns event type (Malfunction/Injury/Death), device brand name, device class, manufacturer, report date, event date, event location, and report source type. Filter using Lucene syntax: device.brand_name:"pacemaker" or event_type:"Death". MAUDE (Manufacturer and User Facility Device Experience) is the primary FDA device safety surveillance database. Source: FDA MAUDE database, US public domain.

Healthprovider: Openfda_devices#openfda_devices#health

Input schema

skip

Number of records to skip for pagination (default 0).

integer
limit

Number of records to return (1–99, default 10).

integer
search

OpenFDA search expression using Lucene syntax. Single field: device_name:"pacemaker" or recall_status:"Ongoing". Combined: device_name:"insulin pump"+AND+recall_status:"Ongoing". Omit to return recent records sorted by date.

string

Call via REST

curl -X POST https://unifyapi.pro/api/call/openfda_devices.adverse_events \
  -H "Authorization: Bearer uak_live_..." \
  -H "Content-Type: application/json" \
  -d '{"skip":0,"limit":0,"search":"<search>"}'

Try it

Paste a UnifyAPI key (create one in the dashboard) and run a real call.