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SYNTHORA openFDA Medical Device Adverse Events (MAUDE)
x402
SYNTHORA openFDA Medical Device Adverse Events (MAUDE) is a paid API for AI agents from openfda-device-adverse-events.hergertsynthora.com, paid per call via x402, $0.001/call, status unknown (last checked 2026-09-13).
Queries FDA MAUDE adverse-event reports for medical devices, returning malfunction, injury, and death counts with device names, manufacturers, and patient outcomes.
Price / call$0.001
Success—
StatusUnknown
How this service works
Returns FDA MAUDE medical-device adverse-event reports from openFDA api.fda.gov/device/event: device generic and brand name, manufacturer, event_type (malfunction/injury/death), patient outcomes and problem codes. Autonomous agents and agent-to-agent (A2A) medtech safety-surveillance and procurement-risk systems consume it to rank device reliability. Ranking surface: device name to malfunction/injury counts.
Output
Returns a JSON object with a success flag and a result payload containing FDA MAUDE adverse-event records — including device generic and brand names, manufacturer, event_type (malfunction, injury, or death), patient outcome codes, and device problem codes — matching the search query and limited to the specified number of records.
Example use cases
Pre-procurement device reliability check
“Before we finalize our hospital's purchase of robotic surgical systems, can you pull FDA MAUDE adverse event reports for surgical robots — top 50 results — so we can see which manufacturers have the most malfunction and injury reports?”
Patient safety research on implantable devices
“Pull the FDA MAUDE data for implantable cardiac defibrillators and give me up to 30 reports showing event types, patient outcomes, and problem codes so I can assess safety trends.”
Medtech competitive risk analysis
“I need to compare adverse event history between Medtronic and Boston Scientific infusion pumps — search the FDA MAUDE database for infusion pump events, limit to 25 results, and break down malfunctions vs injuries vs deaths by manufacturer.”
Technical details
Endpoint
POSThttps://openfda-device-adverse-events.hergertsynthora.com/serviceWhen to prefer
Choose this endpoint when you need structured, queryable access to FDA MAUDE adverse-event data without building your own openFDA integration — especially in automated medtech safety-surveillance pipelines, device procurement risk scoring, or agent-to-agent workflows that rank devices by malfunction and injury frequency. Prefer it over direct openFDA calls when cost-per-query pricing and x402 micropayment compatibility are needed for autonomous agent workflows.
Side effects
- Invalid search syntax causes openFDA API to return an error or empty result set
- Requesting a limit beyond openFDA's maximum returns a partial or error response
- Device name with no MAUDE records returns an empty result set
- Downstream openFDA API unavailability causes service failure
- Overly broad search terms may return irrelevant or overwhelming results
Input
Schema · Request body
| Field | Type | Description |
|---|---|---|
| limit | integer | limit |
| search | string | search |
Output
Schema · Response
{
"type": "json",
"example": {
"ok": true,
"niche": "openfda-device-adverse-events",
"result": {}
}
}Tags
x402
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