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Vinkius

OpenFDA Connector for AI agents.

8 live capabilities

Query drug safety records and food recall data instantly.

Live agent request OpenFDA / Connector

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AI Agent

Why people use OpenFDA

OpenFDA for Real-time Medical Device Recalls

With this Connector, you can just ask your agent about a specific device. It pulls the recall reasons, firm details, and distribution patterns instantly. You get a clear picture of the safety landscape without ever leaving your workspace.

  • Claude
  • ChatGPT
  • Gemini
  • Cursor
  • Visual Studio Code
  • Windsurf

What Vinkius changes

You get direct access to official FDA safety records without the manual research.

Use it from Claude, ChatGPT, Cursor or another AI client you already have.

One account · 5,900+ Connectors

  1. Real-world use case 01

    Analyzing side effect trends

    A researcher asks their agent to pull all reports for a specific medication using search_drug_events to identify common patient reactions like nausea or headaches.

  2. Real-world use case 02

    Rapid food safety checks

    A public health officer asks for all active Class I food recalls to see which products are currently being pulled from shelves.

  3. Real-world use case 03

    Medical device verification

    A procurement specialist uses search_device_clearance to confirm if a new brand of pacemaker has received 510(k) clearance.

Complete set · 8capabilities

The complete OpenFDA capability set.

These are the exact actions your AI can choose when you ask it to work with OpenFDA.

Capability set01 / 02

01—04

4 capabilities in this set.

Part of 8 available through OpenFDA.

  1. 01 Capability

    Search animal events

    Get reports on adverse events for animal drugs and veterinary products. You can filter by species or specific active ingredients.

  2. 02 Capability

    Search device events

    Check reports on medical device malfunctions, injuries, or deaths. Query by brand name or specific patient problems.

  3. 03 Capability

    Search drugsfda

    Find FDA-approved drug applications. Get active ingredients, sponsor info, and approval dates for specific brands or generics.

  4. 04 Capability

    Search drug events

    Pull adverse event reports from healthcare pros and consumers. Filter by reaction type or brand name.

Capability set02 / 02

05—08

4 capabilities in this set.

Part of 8 available through OpenFDA.

  1. 05 Capability

    Search drug labels

    Get structured drug labeling data. Find dosage, warnings, and active ingredients for specific medications.

  2. 06 Capability

    Search food recalls

    Find food product recall enforcement reports. See the reason for the recall and the classification risk level.

  3. 07 Capability

    Search device clearance

    Look up 510(k) premarket clearance data for medical devices. Get names, applicant details, and decision dates.

  4. 08 Capability

    Search device recalls

    Get details on recalled medical devices. See the reason for the recall, the firm involved, and the distribution pattern.

Set up in minutes

One URL. Then ask OpenFDA to work.

Claude and ChatGPT only need the Connector URL. Copy it once, add it in settings, and use OpenFDA from the conversation.

Choose your client

Live preview
Advanced clients IDE · CLI

Claude · Web + desktop

Official guide ↗

Connector URL · ready to paste

Streamable HTTP
https://edge.vinkius.com/vk_preview_drPHoUyEkKpjWhkbglDczVHaC2gLoF9ee58SkHEv/mcp
  1. Step 01

    Open Connectors

    In Claude Web or Claude Desktop, open Settings and choose Connectors.

  2. Step 02

    Add the URL

    Choose Add custom connector, name it OpenFDA, and paste the URL above.

  3. Step 03

    Turn it on in chat

    Select +, open Connectors, and enable OpenFDA for the conversation.

Where the request belongs

Work OpenFDA can move forward.

Built around the request

This is for healthcare professionals, drug researchers, and safety auditors who need to monitor public health data without digging through government databases manually.

01

Pharmacovigilance Researcher

Uses the Connector to quickly pull and summarize adverse event reports for specific drug classes to identify safety trends.

02

Public Health Auditor

Monitors food recall enforcement reports and medical device malfunctions to create safety reports for stakeholders.

03

Medical Device Specialist

Checks 510(k) premarket clearance data and recall reports to verify the status of specific medical technologies.

Bring your own AI

Change the model, client or framework. Keep OpenFDA connected.

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Before you connect

Questions about OpenFDA.

The practical details behind the request, access and result.

Can I use OpenFDA MCP to check for food recalls?

Yes. You can ask your agent to find specific food recalls, and it will pull the reason for the recall, the firm involved, and the risk classification for you.

How does OpenFDA MCP help with drug safety reports?

It lets you query the FAERS database to see what side effects and adverse events are being reported by patients and doctors for specific medications.

Can OpenFDA MCP find medical device malfunctions?

Yes. It can search the MAUDE database for reports of injuries, deaths, and malfunctions related to specific medical devices.

Does OpenFDA MCP require an API key?

No. One of the best things about this Connector is that it works immediately without you needing to sign up for or manage any individual FDA API keys.

Can I use OpenFDA MCP for veterinary drug reports?

Yes. It includes capabilities to search for adverse events related to animal drugs and veterinary products, including reports for specific species like dogs.

How does OpenFDA MCP help researchers analyze drug trends?

Researchers can use it to quickly pull approved drug applications, active ingredients, and approval dates to identify trends in new drug approvals.

Do I need an API key?

No! OpenFDA data is completely free and open. No authentication required. Just subscribe and start searching. Rate limit is 240 requests/minute for unauthenticated access.

What search syntax should I use?

Use Lucene query syntax: openfda.brand_name:"Advil" for brand names, patient.reaction.reactionmeddrapt:"headache" for reactions, event_type:"Injury" for device events. Combine with AND/OR operators.

What are drug adverse events?

Drug adverse events are safety reports submitted to the FDA about potential side effects from medications. Reports come from healthcare professionals, consumers and manufacturers. They do NOT prove the drug caused the event. just that the event was reported while the patient was taking the drug.

One connection away

Give your agent a direct line to OpenFDA.

Connect OpenFDA once. Keep it beside 5,900+ managed Connectors when the next task needs more.

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