Infusion Pump Adverse Event Reports (FDA MAUDE)
Recent FDA device adverse event reports for infusion pumps: report number, event type, dates, device brand and type, manufacturer, product code, model, device and patient problem codes, plus a MAUDE detail link built from the report key so it opens. For device safety, quality engineering and product-liability research. Change the search words to any device type, or filter by event type.
Input
Output fields
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.
