{"uid":"cap_6pPIKhrEyXcg90eHPiRk_","slug":"synthora-openfda-medical-device-adverse-events-maude-a5989953","name":"SYNTHORA openFDA Medical Device Adverse Events (MAUDE)","description":"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.","url":"https://openfda-device-adverse-events.hergertsynthora.com/service","method":"POST","headers":{},"bodySchema":{"type":"object","properties":{"limit":{"type":"integer","description":"limit"},"search":{"type":"string","description":"search"}}},"responseSchema":{"type":"json","example":{"ok":true,"niche":"openfda-device-adverse-events","result":{}}},"example":null,"exampleRequest":null,"tags":["x402"],"displayCostAmount":"0.001","displayCostAsset":"USDC","priceDynamic":false,"priceHint":null,"priceStatus":"priced","priceSource":"probe","requiresHandshake":false,"reviewCount":0,"rating":{"score":"0.00","successRate":"0.00","reviews":0,"stars":null,"state":"unrated"},"availabilityStatus":"unknown","priceObserved":null,"sessionDeposit":null,"pricing":{"kind":"static","summary":"$0.001/call","primary":{"kind":"static","protocol":"x402","network":"base","amountUsd":"0.001","per":"call","confidence":"exact"},"accepted":[{"kind":"static","protocol":"x402","network":"base","amountUsd":"0.001","per":"call","confidence":"exact"}]},"paymentMethods":[{"uid":"pm_eHkJpEw4pkeZYswgQ_Inx","protocol":"x402","methodType":"crypto","chain":"base","mode":"charge","costAmount":"0.001","costPer":"request","priority":0,"asset":"0x833589fCD6eDb6E08f4c7C32D4f71b54bdA02913","unit":"request","depositMicros":null,"planRef":null}],"brandName":null,"brandSlug":null,"brandBaseUrl":null,"brandDocsUrl":null,"whatItDoes":"Queries FDA MAUDE adverse-event reports for medical devices, returning malfunction, injury, and death counts with device names, manufacturers, and patient outcomes.","exampleAgentPrompt":"Search the FDA MAUDE database for adverse event reports on insulin pumps — show me the top 20 results including device name, manufacturer, and whether events were malfunctions, injuries, or deaths.","exampleUseCases":[{"title":"Pre-procurement device reliability check","prompt":"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?"},{"title":"Patient safety research on implantable devices","prompt":"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."},{"title":"Medtech competitive risk analysis","prompt":"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."}],"resultDescription":"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.","failureModes":["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"],"whenToPreferThis":"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.","instructions":null,"reviewSummary":null,"reviewSummaryHighlights":null,"reviewSummaryConcerns":null,"reviewSummaryGeneratedAt":null,"activationCount":0,"lastUsedAt":null,"lastSuccessfullyRanAt":null,"lastHealthCheckAt":"2026-09-16T00:33:26.668Z","isFirstParty":false}