{"uid":"cap_N2W1_kyhBZ3wgPMvdAuwe","slug":"2s-io-2d68b2f9","name":"FDA Medical Device Adverse Event Reports (MAUDE) via 2s.io","description":"FDA medical device adverse event reports (MAUDE), newest first by date received. All filters optional. Each record includes report number, event type, dates received + of event, manufacturer, brand/generic device name, model + catalog numbers, listed device problems, patient outcomes, and primary narrative text. Backed by OpenFDA's /device/event endpoint; public-domain US government records.","url":"https://2s.io/api/gov/fda-device-events","method":"GET","headers":{},"bodySchema":{"type":"object","$schema":"https://json-schema.org/draft/2020-12/schema","required":["input"],"properties":{"input":{"type":"object","required":["type","method","queryParams"],"properties":{"type":{"const":"http"},"method":{"const":"GET"},"queryParams":{"type":"object","properties":{"limit":{"type":"integer","default":20,"maximum":100,"minimum":1,"description":"Max events (1-100). Default 20."},"device":{"type":"string","maxLength":100,"minLength":2,"description":"Device-name substring across brand_name + generic_name. Examples: \"pacemaker\", \"insulin pump\", \"DePuy hip\"."},"problem":{"type":"string","maxLength":100,"minLength":2,"description":"FDA device product code substring (advanced filter; most users want device or manufacturer)."},"manufacturer":{"type":"string","maxLength":100,"minLength":2,"description":"Manufacturer-name substring. Examples: \"medtronic\", \"boston scientific\", \"abbott\"."}},"additionalProperties":false}}}}},"responseSchema":null,"example":{"request":{"input":{"type":"http","method":"GET","queryParams":{"limit":10,"device":"pacemaker"}}},"response":{"data":{"ok":true,"meta":{"query":{"limit":10,"device":"pacemaker","problem":null,"manufacturer":null}},"items":[{"brandName":"CAPSUREFIX NOVUS LEAD MRI SURESCAN","eventType":"Injury","dateOfEvent":"2026-05-08","genericName":"PERMANENT PACEMAKER ELECTRODE","modelNumber":"5076-52","dateReceived":"2026-05-31","reportNumber":"3008973940-2026-04090","catalogNumber":"5076-52","deviceProblems":[],"patientOutcome":[],"eventDescription":null,"manufacturerName":null},{"brandName":"ASSURITY MRI","eventType":"Malfunction","dateOfEvent":null,"genericName":"Implantable pulse generator, pacemaker (non-CRT)","modelNumber":"PM2272","dateReceived":"2026-05-31","reportNumber":"2017865-2026-11259","catalogNumber":"","deviceProblems":[],"patientOutcome":[],"eventDescription":null,"manufacturerName":null},{"brandName":"KORA","eventType":"Malfunction","dateOfEvent":"2026-04-30","genericName":"IMPLANTABLE PULSE GENERATOR, PACEMAKER (NON-CRT)","modelNumber":"KORA 250 DR","dateReceived":"2026-05-31","reportNumber":"1000165971-2026-00998","catalogNumber":"TPM010C","deviceProblems":[],"patientOutcome":[],"eventDescription":null,"manufacturerName":null},{"brandName":"ASSURITY MRI","eventType":"Malfunction","dateOfEvent":"2026-05-08","genericName":"Implantable pulse generator, pacemaker (non-CRT)","modelNumber":"PM1272","dateReceived":"2026-05-31","reportNumber":"2017865-2026-11260","catalogNumber":"","deviceProblems":[],"patientOutcome":[],"eventDescription":null,"manufacturerName":null},{"brandName":"ACCOLADE? MRI EL DR","eventType":"Malfunction","dateOfEvent":"2026-05-05","genericName":"PACEMAKER","modelNumber":"L331","dateReceived":"2026-05-29","reportNumber":"2124215-2026-28855","catalogNumber":"L331","deviceProblems":[],"patientOutcome":[],"eventDescription":"IT WAS REPORTED THAT THE PATIENT WITH THIS PACEMAKER EXPERIENCED ELEVATED HEART RATES IN THE 130 BEATS PER MINUTE (BPM) RANGE DURING MINIMAL PHYSICAL ACTIVITY. TECHNICAL SERVICES (TS) REVIEWED THE DEVICE SETTINGS AND NOTED THAT THE MINUTE VENTILATION (MV) AND ACCELEROMETER SENSOR RATE WERE APPROPRIATELY PROGRAMMED TO A MAXIMUM OF 130 BPM. THE PATIENT ALSO HAD A HISTORY OF RIGHT ATRIAL (RA) LEAD NOISE AND SIGNAL ARTIFACT MONITOR (SAM) EPISODES WERE OBSERVED WHERE THE NOISE WAS OVERSENSED. TS DISCUSSED POTENTIAL REPROGRAMMING ADJUSTMENTS, REDUCING OR DISABLING MINUTE VENTILATION RESPONSE IF NEEDED.  NO ADVERSE PATIENT EFFECTS WERE REPORTED. THIS PACEMAKER REMAINS IN SERVICE.","manufacturerName":null},{"brandName":"INGEVITY+","eventType":"Injury","dateOfEvent":"2026-04-01","genericName":"DRUG ELUTING PERMANENT RIGHT VENTRICULAR OR ATRIAL PACEMAKER ELECTRODES","modelNumber":"7841","dateReceived":"2026-05-29","reportNumber":"2124215-2026-28788","catalogNumber":"7841","deviceProblems":[],"patientOutcome":["Hospitalization"," R"],"eventDescription":"IT WAS REPORTED THAT THIS RIGHT ATRIAL (RA) LEAD WAS EXPLANTED DUE TO AN ALLEGATION OF BEING DAMAGED. NO ADDITIONAL ADVERSE PATIENT EFFECTS WERE REPORTED.","manufacturerName":null},{"brandName":"ESSENTIO MRI DR","eventType":"Malfunction","dateOfEvent":"2026-03-10","genericName":"PACEMAKER","modelNumber":"L111","dateReceived":"2026-05-29","reportNumber":"2124215-2026-28820","catalogNumber":"L111","deviceProblems":[],"patientOutcome":[],"eventDescription":"IF PERTINENT INFORMATION IS PROVIDED IN THE FUTURE, A SUPPLEMENTAL REPORT WILL BE SUBMITTED.","manufacturerName":null},{"brandName":"ASSURITY MRI","eventType":"Malfunction","dateOfEvent":"2026-05-08","genericName":"Implantable pulse generator, pacemaker (non-CRT)","modelNumber":"PM2272","dateReceived":"2026-05-29","reportNumber":"2017865-2026-11170","catalogNumber":"","deviceProblems":[],"patientOutcome":[],"eventDescription":"IT WAS REPORTED THAT THE PATIENT PRESENTED FOR AN IMPLANT PROCEDURE OF A DUAL CHAMBER PACEMAKER. DURING THE PROCEDURE, THE PHYSICIAN COULD NOT EXTEND THE SCREW IN THE HEADER FOR THE RIGHT VENTRICULAR PORT. HE COULD NOT GET THE SCREW BACK AND THE LEAD OUT OF THE HEADER. THE PACEMAKER WAS NOT USED AND REPLACED. THE PATIENT WAS IN STABLE CONDITION.","manufacturerName":null},{"brandName":"CARELINK PROGRAMMER","eventType":"Malfunction","dateOfEvent":"2026-05-08","genericName":"PROGRAMMER, PACEMAKER","modelNumber":"2090","dateReceived":"2026-05-29","reportNumber":"2182208-2026-31595","catalogNumber":"2090","deviceProblems":[],"patientOutcome":[],"eventDescription":null,"manufacturerName":null},{"brandName":"CAPSUREFIX NOVUS LEAD MRI SURESCAN","eventType":"Injury","dateOfEvent":"2026-05-21","genericName":"PERMANENT PACEMAKER ELECTRODE","modelNumber":"5076-58","dateReceived":"2026-05-29","reportNumber":"2649622-2026-15927","catalogNumber":"5076-58","deviceProblems":[],"patientOutcome":["Required Intervention"," H"],"eventDescription":"MEDTRONIC SUBMITS THIS REPORT TO COMPLY WITH FDA REGULATIONS 21 CFR PARTS 4 AND 803. MEDTRONIC HAS MADE REASONABLE EFFORTS TO PROVIDE AS MUCH RELEVANT INFORMATION AS IS AVAILABLE TO THE COMPANY AS OF THE SUBMISSION DATE OF THIS REPORT. THIS REPORT DOES NOT CONSTITUTE AN ADMISSION OR A CONCLUSION BY FDA, MEDTRONIC, OR ITS EMPLOYEES THAT THE DEVICE, MEDTRONIC, OR ITS EMPLOYEE CAUSED OR CONTRIBUTED TO THE EVENT DESCRIBED IN THE REPORT. ANY REQUIRED FIELDS THAT ARE UNPOPULATED ARE BLANK BECAUSE THE INFORMATION IS CURRENTLY UNKNOWN OR UNAVAILABLE. MEDTRONIC WILL SUBMIT A SUPPLEMENTAL REPORT IF ADDITIONAL RELEVANT INFORMATION BECOMES KNOWN.","manufacturerName":null}],"total":719005,"source":{"url":"https://open.fda.gov/apis/device/event/","license":"Public domain (US government records)","provider":"OpenFDA — Medical Device Adverse Event Reports (MAUDE)"}},"meta":{"cost":{"usd":0.0024,"tier":0},"caller":"x402","version":null,"endpoint":"gov.fda-device-events","settlement":{"txHash":"0x584e3e958ed257ac3cff5fca4cf2ab683e6ba1914775b9bbc1f93726aef1f661","network":"eip155:8453","success":true}}}},"exampleRequest":{"limit":10,"device":"pacemaker"},"tags":["x402"],"displayCostAmount":"0.0024","displayCostAsset":"USDC","priceDynamic":false,"priceHint":null,"priceStatus":"priced","priceSource":"settled","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":"$0.0024/call","primary":{"kind":"static","protocol":"x402","network":"base","amountUsd":"0.006","per":"call","confidence":"exact"},"accepted":[{"kind":"static","protocol":"x402","network":"base","amountUsd":"0.006","per":"call","confidence":"exact"}]},"paymentMethods":[{"uid":"pm_bFqlSBxzRvpKKNjyDdzKE","protocol":"x402","methodType":"crypto","chain":"base","mode":"charge","costAmount":"0.006","costPer":"request","priority":0,"asset":"0x833589fCD6eDb6E08f4c7C32D4f71b54bdA02913","unit":"request","depositMicros":null,"planRef":null}],"brandName":null,"brandSlug":null,"brandBaseUrl":null,"brandDocsUrl":null,"whatItDoes":"Returns FDA MAUDE adverse event reports for medical devices, newest first, filterable by device name, manufacturer, or product code.","exampleAgentPrompt":"Can you pull the 10 most recent FDA MAUDE adverse event reports for DePuy hip implants from Medtronic and summarize the reported device problems and patient outcomes?","exampleUseCases":null,"resultDescription":"A list of MAUDE adverse event report records, newest first, each containing the report number, event type, dates received and of the event, manufacturer name, brand and generic device name, model and catalog numbers, listed device problems, patient outcomes, and primary narrative text. Up to 100 records per call, default 20.","failureModes":["Device or manufacturer substring matches no records — returns empty result set","Limit value out of range (must be 1–100) — validation error","OpenFDA upstream unavailable — gateway or timeout error","Too-broad query returning irrelevant results due to substring matching across many brands"],"whenToPreferThis":"Use this endpoint when you need structured FDA MAUDE adverse event data for a specific medical device or manufacturer, particularly when you want pre-parsed fields (report number, event type, patient outcomes, narrative) rather than raw OpenFDA JSON. Prefer over direct OpenFDA calls when operating in an agentic/x402 pay-per-call context needing convenience and clean output.","instructions":null,"reviewSummary":null,"reviewSummaryHighlights":null,"reviewSummaryConcerns":null,"reviewSummaryGeneratedAt":null,"activationCount":0,"lastUsedAt":null,"lastSuccessfullyRanAt":null,"lastHealthCheckAt":"2026-09-14T00:57:12.466Z","isFirstParty":false}