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openfda_devices.safety.adverse_events

Search FDA MAUDE database for medical device adverse event reports — 25M+ records of device malfunctions, injuries, and deaths. Returns event type (Malfunction/Injury/Death), device brand name, device class, manufacturer, report date, event date, event location, and report source type. Filter usi...

SERVERApibase SOURCEapibase-mcp-client
Low RISK CLASS
Category Read
Parameters 30 required
Recommended Allowedsee the rule below
Registry record Grade F, identity unverified Pull the record →

This record as markdown: /tools/io-github-whiteknightonhorse-apibase/openfda-devices.safety.adverse-events.md

What openfda_devices.safety.adverse_events does on Apibase

AI agents call openfda_devices.safety.adverse_events to retrieve information from Apibase without modifying anything. It is typically the context-gathering step in research, monitoring, and reporting workflows, before the agent takes action elsewhere.

ParameterTypeRequiredDescription
skip integer — Number of records to skip for pagination (default 0).
limit integer — Number of records to return (1–99, default 10).
search string — OpenFDA search expression using Lucene syntax. Single field: device_name:"pacemaker" or recall_status:"Ongoing". Combined: device_name:"insulin pump"+AND+recall

Parameters from the server's own tool schema.

Why openfda_devices.safety.adverse_events is rated Low

Tool retrieves publicly available FDA safety data without modifying, executing, or deleting anything.

From the tool's definition Search FDA MAUDE database for medical device adverse event reports — 25M+ records

Questions about openfda_devices.safety.adverse_events

What does the openfda_devices.safety.adverse_events tool do? +

Search FDA MAUDE database for medical device adverse event reports — 25M+ records of device malfunctions, injuries, and deaths. Returns event type (Malfunction/Injury/Death), device brand name, device class, manufacturer, report date, event date, event location, and report source type. Filter using Lucene syntax: device.brand_name:"pacemaker" or event_type:"Death". MAUDE (Manufacturer and User Facility Device Experience) is the primary FDA device safety surveillance database. Source: FDA MAUDE database, US public domain. It is categorised as a Read tool in the Apibase MCP Server, which means it retrieves data without modifying state.

What parameters does openfda_devices.safety.adverse_events accept? +

openfda_devices.safety.adverse_events accepts 3 parameters: skip, limit, search. The full parameter table on this page comes from the server's own tool schema.

How do I enforce a policy on openfda_devices.safety.adverse_events? +

Register the Apibase MCP server in PolicyLayer and add a rule for openfda_devices.safety.adverse_events: allow, deny, rate-limit, or require approval. Point your MCP client at the PolicyLayer proxy URL and the rule is enforced on every call, before it reaches Apibase. Nothing to install.

What risk level is openfda_devices.safety.adverse_events? +

openfda_devices.safety.adverse_events is a Read tool with low risk. Read-only tools are generally safe to allow by default.

Can I rate-limit openfda_devices.safety.adverse_events? +

Yes. Add a rate_limit block to the openfda_devices.safety.adverse_events rule in your PolicyLayer policy. For example, setting max: 10 and window: 60 limits the tool to 10 calls per minute. Rate limits are tracked per agent session and reset automatically.

How do I block openfda_devices.safety.adverse_events completely? +

Set action: deny in the PolicyLayer policy for openfda_devices.safety.adverse_events. The AI agent will receive a policy violation error and cannot call the tool. You can also include a reason field to explain why the tool is blocked.

What MCP server provides openfda_devices.safety.adverse_events? +

openfda_devices.safety.adverse_events is provided by the Apibase MCP server (apibase-mcp-client). PolicyLayer sits as a proxy in front of this server to enforce policies before tool calls reach the server.

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