FDA medical device adverse event reports (MAUDE), newest...
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.
Request
- Base URL: https://2s.io
- URL: https://2s.io/api/gov/fda-device-events
- Auth: API key in header PAYMENT-SIGNATURE
Query parameters
Device-name substring across brand_name + generic_name. Examples: "pacemaker", "insulin pump", "DePuy hip".
Manufacturer-name substring. Examples: "medtronic", "boston scientific", "abbott".
FDA device product code substring (advanced filter; most users want device or manufacturer).
Max events (1-100). Default 20.
Try before you buy. Set to 1 for one free real call per endpoint per hour — no wallet or payment needed — to verify the endpoint before paying. Equivalent to sending the "X-2s-Trial: 1" request header. Listed only on operations that offer a trial; the others always answer 402.
Response
Changes
No recorded changes to this operation across all 1 revision of this API.