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
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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, search words, and more, to match your specific use case.
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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.
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The final output is delivered in JSON, CSV, or Excel format, ready to be plugged into your workflow. You can also run the "Infusion Pump Adverse Event Reports (FDA MAUDE)" task via API.
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