{"uid":"cap_K0BkQF-pfN6z_j6i_qXZd","slug":"fda-device-adverse-events-lookup-d2a9f4e2","name":"FDA Device Adverse Events Lookup","description":"Summarize FDA medical device adverse event reports (openFDA MAUDE) for a device name, brand, product code or manufacturer: total matching reports, counts by event type (death, injury, malfunction), the most reported device problems, and the newest reports with date, event type, device, manufacturer, problems and a short excerpt of the event description. Counts cover every matching report; the report list is a capped sample and says so. Optional since date. Live FDA data, no key.","url":"https://agent402.tools/api/device-adverse-events?utm_source=zero.xyz","method":"GET","headers":{},"bodySchema":{"type":"object","$schema":"https://json-schema.org/draft/2020-12/schema","required":["input"],"properties":{"input":{"type":"object","required":["type","method"],"properties":{"type":{"type":"string","const":"http"},"method":{"enum":["GET"],"type":"string"},"queryParams":{"type":"object","required":[],"properties":{"brand":{"type":"string","description":"Brand name as reported"},"limit":{"type":"number","description":"Newest reports to list, 0-10 (default 5)"},"since":{"type":"string","description":"Only reports received on or after this date (YYYY-MM-DD)"},"device":{"type":"string","description":"Generic device name as reported, e.g. insulin pump"},"problems":{"type":"number","description":"Top device problems to rank, 1-25 (default 10)"},"productCode":{"type":"string","description":"Three-letter FDA product code, e.g. LZG"},"manufacturer":{"type":"string","description":"Device manufacturer name as reported"}}}},"additionalProperties":false},"output":{"type":"object","required":["type"],"properties":{"type":{"type":"string"},"example":{"type":"object"}}}}},"responseSchema":{"type":"json","example":{"query":{"brand":null,"since":null,"device":"insulin pump","productCode":null,"manufacturer":null},"source":"api.fda.gov (openFDA device adverse events, public domain)","matched":171622,"complete":false,"returned":1,"truncated":true,"disclaimer":"openFDA data is unvalidated and is not medical advice; do not rely on it to make decisions regarding medical care.","eventTypes":[{"reports":120000,"eventType":"Malfunction"},{"reports":50000,"eventType":"Injury"},{"reports":300,"eventType":"Death"}],"topProblems":[{"problem":"Unintended Movement","reports":41009}],"totalReports":171622,"recentReports":[{"excerpt":"IT WAS REPORTED THAT THE PUMP ...","problems":["Unintended Movement"],"brandName":"EXAMPLE PUMP","eventType":"Malfunction","dateOfEvent":"2026-09-20","deviceClass":"2","genericName":"INSULIN PUMP","productCode":"LZG","dateReceived":"2026-10-01","excerptChars":640,"manufacturer":"Example Medical","mdrReportKey":"21000000","reportNumber":"2032227-2026-01234","excerptTruncated":true}],"maxExcerptChars":280}},"example":null,"exampleRequest":null,"tags":["x402"],"displayCostAmount":"0.004","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":"$0.004/call","primary":{"kind":"static","protocol":"x402","network":"base","amountUsd":"0.004","per":"call","confidence":"exact"},"accepted":[{"kind":"static","protocol":"x402","network":"base","amountUsd":"0.004","per":"call","confidence":"exact"}]},"paymentMethods":[{"uid":"pm_kEAspEJdLU2Z9LgQGrzQ5","protocol":"x402","methodType":"crypto","chain":"base","mode":"charge","costAmount":"0.004","costPer":"request","priority":0,"asset":"0x833589fCD6eDb6E08f4c7C32D4f71b54bdA02913","unit":"request","depositMicros":null,"planRef":null}],"brandName":null,"brandSlug":null,"brandBaseUrl":null,"brandDocsUrl":null,"whatItDoes":"Queries the FDA MAUDE database to summarize adverse event reports for a medical device, returning total counts, event type breakdowns, top device problems, and recent report excerpts.","exampleAgentPrompt":"Can you pull up the FDA adverse event reports for insulin pumps — I want to see the total number of reports, how many were deaths, injuries, or malfunctions, the top 10 device problems, and the 5 most recent reports since January 2023?","exampleUseCases":[{"title":"Pre-purchase medical device safety check","prompt":"Before we recommend this CPAP brand to patients, can you look up FDA adverse event reports for ResMed AirSense and show me the total reports, how many were serious injuries or deaths, and what the most common device problems are?"},{"title":"Regulatory due diligence by product code","prompt":"I need a safety summary for the FDA product code LZG — give me total adverse event counts broken down by death, injury, and malfunction, the top 15 device problems, and the 5 newest report excerpts."},{"title":"Post-market surveillance for a manufacturer","prompt":"Can you pull FDA MAUDE data for all devices made by Boston Scientific and show me the breakdown of event types plus the most frequently reported problems? Only include reports from 2022 onwards."}],"resultDescription":"Returns a structured summary including: total count of matching FDA adverse event reports, counts broken down by event type (death, injury, malfunction), a ranked list of the most frequently reported device problems (up to 25), and a capped sample of the newest reports each containing the report date, event type, device name, manufacturer, problem list, and a short excerpt of the event description.","failureModes":["No results found if device name or brand does not match FDA MAUDE records exactly","Ambiguous device names may return overly broad or irrelevant results","since date in wrong format causes query failure","productCode must be exactly 3 letters or query fails","FDA API downtime may result in no data returned","Rate limiting or upstream FDA service errors may produce empty responses"],"whenToPreferThis":"Use this endpoint when you need structured, pre-summarized adverse event intelligence from the FDA MAUDE database without needing an FDA API key. It is ideal for agents performing safety due diligence on specific devices, brands, or manufacturers — especially when you want aggregated counts plus recent report excerpts in a single call. Prefer this over raw FDA API queries when you need a ready-to-use summary rather than raw JSON, and when the device can be identified by name, brand, product code, or manufacturer.","instructions":null,"reviewSummary":null,"reviewSummaryHighlights":null,"reviewSummaryConcerns":null,"reviewSummaryGeneratedAt":null,"activationCount":0,"lastUsedAt":null,"lastSuccessfullyRanAt":null,"lastHealthCheckAt":"2026-10-30T19:06:34.640Z","isFirstParty":false,"canonicalSlug":"fda-device-adverse-events-lookup-d2a9f4e2"}