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FDA Device Injury Reports by Product Code (MAUDE)

FDA MAUDE adverse event reports of type Injury for one FDA device product code: report number, dates, device brand and type, manufacturer, model, problem codes, and a MAUDE detail link built from the report key so it opens. For device safety and quality engineers who already know the three-letter FDA product code for their device type. Change the code and the event type, e.g. Death or Malfunction.

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openFDA API: FDA Recalls, Drug Labels & Device Reports
openFDA API: FDA Recalls, Drug Labels & Device Reportsyadroo/openfda-records
Report number
Event type
Date received
Date of event
+7 fields
Text
Number
Boolean
List
Object

Input

What to fetch:deviceEvents
Device product code:QFG
Device event types:Injury
Max rows:15

Output fields

Report number
Event type
Date received
Date of event
Device brand
Device type
Device manufacturer
Product code
Device problems
Patient problems
Detail page

How it works

Sign up on Apify or log in

The openFDA API: FDA Recalls, Drug Labels & Device Reports Actor is ready to run with the inputs already set for "FDA Device Injury Reports by Product Code (MAUDE)". Sign up or log in and you'll land in Apify Console with a copy of this exact task.

Start the "FDA Device Injury Reports by Product Code (MAUDE)" task

The openFDA API: FDA Recalls, Drug Labels & Device Reports Actor will start running based on the input automatically. You can also change all the input fields, like what to fetch, device product code, and more, to match your specific use case.

Receive the "FDA Device Injury Reports by Product Code (MAUDE)" output

Monitor the progress in real time. You will be notified as soon as your dataset is complete and ready for review. Each result includes data such as report number, event type, date received, and more.

Integrate into your workflow

The final output is delivered in JSON, CSV, or Excel format, ready to be plugged into your workflow. You can also run the "FDA Device Injury Reports by Product Code (MAUDE)" task via API.

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