FDA Medical Device Shortages & Discontinuance List Actor

FDA Medical Device Recall Search

ryanclinton/fda-device-recalls

FDA Medical Device Recall Search queries the U.S. Food and Drug Administration's openFDA device enforcement endpoint to retrieve detailed, structured data about medical device recalls.

FDA Medical Device Recalls Scraper

automation-lab/fda-medical-device-recalls-scraper

Extract official FDA medical device recall records from openFDA by firm, product, class, status, location, and date. Export JSON, CSV, or Excel.

Query FDA MAUDE adverse events, 510(k) clearances, and device recalls. One tool call for AI agent medical device compliance research.

Extract FDA medical device UDI records for device identification, product-code enrichment, manufacturer intelligence, and compliance workflows.

FDA Device Recall Intelligence

skootle/fda-device-recall-intelligence

Official openFDA medical device recalls with product codes, device classes, K numbers, firms, root causes, actions, API output, schedules, monitoring, and integrations.

Track FDA medical device 510(k) clearances and recalls from official openFDA data: applicant, device, product code, class, decision date, and Class I/II/III recall severity. For medtech intelligence.

openFDA Medical Device Adverse Events & Recalls Scraper

scrapers_lat/openfda-device-events-scraper

Scrape FDA medical device adverse events (MAUDE), device recalls and 510(k) clearances from the official openFDA API. Extract report number, device brand, manufacturer, event type, product problems and dates across the United States. Export to JSON, CSV or Excel.

FDA Device Recalls — MedTech CI & PV Lookup API

azureblue/medical-device-recall-scraper

Fetch FDA medical device recall records via OpenFDA. Filter by device name and date. Returns recall number, reason, risk class, company and recall status.

Lead lists of FDA-registered medical device establishments: filter by state, product code, and establishment type, and get one row per firm with address, the official correspondent's name and phone, and the devices it makes. Keyless official FDA API, no browser. Pay per manufacturer.

Scrapes FDA's official list of AI/ML-enabled medical devices authorized for U.S. marketing into structured records.