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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".
openFDA API: FDA Recalls, Drug Labels & Device Reportsyadroo/openfda-records
Recall number
Area
Class
Status
+8 fieldsTextNumberBooleanListObject
Input
What to fetch:recalls
Recalls: product area:device
Search words:pacemaker
Search in:product
Only the last N days:365
Max rows:15
Output fields
Recall number
Area
Class
Status
Product
Reason
Recalling firm
State
Distribution
Initiated
Reported
openFDA record
Sign up on Apify01
Create your Apify account to access the openFDA API: FDA Recalls, Drug Labels & Device Reports.
Start the run02
The Actor will start running based on the input automatically.
Receive the output03
Monitor the progress in real-time. You will be notified as soon as your dataset is complete and ready for review.
Integrate into your workflow04
The final output is delivered in JSON, CSV, or Excel format, ready to be plugged into your workflow.
