/openfda/device/events
/openfda/device
/openfda/device/events
Get an FDA MAUDE device adverse-event report by its report number
Price: 1 credit
💡 AI Hint: Get an FDA MAUDE (Manufacturer and User Facility Device Experience) adverse-event report by its report number. Returns the event type and location, key dates, the devices involved (brand, generic and manufacturer names, model, product code, implant flag and openfda block), the patients (age, sex, outcomes) and the MDR narrative texts.
⚠️ Common errors: 412: Device event not found
POST
/openfda/device/events
Authorizations
API token from the dashboard
Headers
Body
application/json
Response
Successful Response