FDA MAUDE Medical Device Adverse Events Scraper API
Pricing
from $2.00 / 1,000 fda maude medical device adverse events scraper ap evidence items
FDA MAUDE Medical Device Adverse Events Scraper API
Search FDA MAUDE adverse-event reports by report, manufacturer, device, product code, event, dates, patient outcome, and device problem. Returns source-linked nested device and patient evidence with mandatory non-causation limits.
Pricing
from $2.00 / 1,000 fda maude medical device adverse events scraper ap evidence items
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Ava Torres
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Search the FDA MAUDE report collection through the official, no-key openFDA Device Event API. This paid actor returns normalized, source-linked event records with stable nested device, patient, product-problem, and narrative evidence.
Fast default and price
The default searches genericName: "Infusion Pump" plus eventType: "Malfunction", sorts by FDA received date descending, and returns one report. Maximum first-run charge is $0.0021: $0.0001 start + $0.002 for one dataset item. maxResults is a total response cap (1–1,000), and an Apify maximum-charge budget can lower it before source pagination.
Manufacturer/device-problem example:
Exact report lookup:
Filters
Report number, manufacturer, brand name, FDA device name, generic name, FDA product code, event type, FDA received-date range, reported patient outcome, and reported device/product problem. Populated filters are combined with AND. Results are newest-first, paginated within explicit bounds, and capped by total maxResults.
Output
Each found item includes report/MDR identifiers, report and event dates, event/report types, manufacturer, product problems, nested devices (brand, generic name, manufacturer, product code, model/catalog/lot, UDI and FDA classification), nested patient outcomes/problems/treatments, narratives, retrieval time, exact API record URL, query bounds, and evidence notices. NO_MATCH, INVALID_INPUT, and SOURCE_UNAVAILABLE are explicit evidence records instead of silent empty runs (except when a buyer charge cap affords zero paid items).
Required interpretation limits
MAUDE includes mandatory and voluntary reports submitted to FDA. A report does not establish causation, incidence rates, a device defect, recall status, or clinical risk. Reports can be incomplete, duplicated, corrected, delayed, or unverified. A missing result does not prove no report exists. MAUDE is not a complete denominator, real-time safety feed, recall database, clinical recommendation, or FDA endorsement. Review the linked FDA record and relevant FDA recall/safety sources before making decisions.
