FDA Pacemaker Device Recall Reports
FDA device recall enforcement reports for one device family (pacemaker by default): recall number, device description, reason for recall, class, status, recalling firm and state, dates, and a link to the openFDA record. For hospital biomedical engineering and device distributors tracking one device type. Change the search words to any device family, e.g. "insulin pump".
Input
Output fields
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 Pacemaker Device Recall Reports". Sign up or log in and you'll land in Apify Console with a copy of this exact task.
Start the "FDA Pacemaker Device Recall Reports" 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, recalls: product area, and more, to match your specific use case.
Receive the "FDA Pacemaker Device Recall Reports" 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 recall number, product area, recall class, 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 Pacemaker Device Recall Reports" task via API.
