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gov_recalls

Product recalls across FDA, USDA, and CPSC in one normalized schema. openFDA enforcement reports (food/drug/device), USDA FSIS recalls, and CPSC consumer-product recalls normalized to one shape with a unified severity class (I highest — FDA/USDA classes verbatim; CPSC derived from hazard language). Newest first. [HTTP: GET /v1/recalls · price $0.01 via x402 · docs https://x402-factory.com/docs/gov.recalls]

Input Schema

TableJSON Schema
NameRequiredDescriptionDefault
qNoMatch against product, brand, or hazard
limitYes
sinceNo
categoryNo

Schema Changelog

Changes observed during successful MCP inspections.

  1. First observed

TDQS

B3.4/5.0
Behavior4/5

Does the description disclose side effects, auth requirements, rate limits, or destructive behavior?

With no annotations, the description carries the full burden and does meaningfully disclose behavior: cross-source normalization into one shape, a unified severity class with stated derivation rules (Class I highest, FDA/USDA verbatim, CPSC derived from hazard language), newest-first ordering, and the HTTP/pricing/auth context (GET /v1/recalls, $0.01 via x402). It omits rate limits and error/empty-result behavior.

Agents need to know what a tool does to the world before calling it. Descriptions should go beyond structured annotations to explain consequences.

Conciseness4/5

Is the description appropriately sized, front-loaded, and free of redundancy?

Front-loaded with the core purpose and normalization model, with pricing/docs demoted to a bracketed footer. Dense but every clause earns its place; the severity-class digression is slightly heavy for a description but still informative.

Shorter descriptions cost fewer tokens and are easier for agents to parse. Every sentence should earn its place.

Completeness3/5

Given the tool's complexity, does the description cover enough for an agent to succeed on first attempt?

Given 4 params, no output schema, no annotations, and low schema coverage, the description adequately covers sources, normalization, and severity but leaves the agent without record-shape or three-of-four parameter explanations. Adequate but with clear gaps for a tool whose structured metadata is thin.

Complex tools with many parameters or behaviors need more documentation. Simple tools need less. This dimension scales expectations accordingly.

Parameters2/5

Does the description clarify parameter syntax, constraints, interactions, or defaults beyond what the schema provides?

Schema description coverage is only 25% (only q is documented), so the description must compensate and does not. It adds no meaning for limit, since, or category, and notably never explains the 'vehicle' enum value, which the three named sources (FDA/USDA/CPSC) do not obviously cover.

Input schemas describe structure but not intent. Descriptions should explain non-obvious parameter relationships and valid value ranges.

Purpose4/5

Does the description clearly state what the tool does and how it differs from similar tools?

States a specific resource (product recalls) and scope (FDA, USDA, CPSC aggregated into one normalized schema), clearly indicating this is the cross-agency tool. It does not name or contrast the category-specific siblings (gov_recalls_food, gov_recalls_drug, etc.), so differentiation is implied rather than explicit.

Agents choose between tools based on descriptions. A clear purpose with a specific verb and resource helps agents select the right tool.

Usage Guidelines3/5

Does the description explain when to use this tool, when not to, or what alternatives exist?

Usage is only implied: covering all three agencies signals this is the general fallback vs the per-category siblings, and 'Newest first' gives ordering context. There is no explicit when-to-use/when-not guidance and no routing to the six category-specific recall tools, which is a notable gap.

Agents often have multiple tools that could apply. Explicit usage guidance like "use X instead of Y when Z" prevents misuse.

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