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Glama

Forget

forget
DestructiveIdempotent

Delete a previously stored memory by key. Use when context is stale, the task is done, or you want to clear sensitive data the agent saved earlier. Pair with remember and recall.

Input Schema

TableJSON Schema
NameRequiredDescriptionDefault
keyYesMemory key to delete

Schema Changelog

Changes observed during successful MCP inspections. Dates show when Glama detected each change.

  1. First observed

TDQS

A4.3/5.0
Behavior3/5

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

Annotations provide destructiveHint and idempotentHint. Description adds 'Delete' which aligns with destructiveHint but does not clarify behavior on missing key or idempotency. No contradiction as description omits detail but does not contradict annotations.

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

Conciseness5/5

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

Two sentences, no waste. Purpose and usage are front-loaded. Every sentence earns its place.

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

Completeness5/5

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

For a simple delete operation with one parameter, no output schema, and comprehensive annotations, the description provides sufficient context including usage guidance and tool pairing.

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

Parameters3/5

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

Schema coverage is 100% with one parameter 'key' described as 'Memory key to delete'. Description adds no extra semantic value beyond the schema, so baseline 3 applies.

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

Purpose5/5

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

Description clearly states 'Delete a previously stored memory by key' with specific verb and resource. It implicitly distinguishes from sibling tools 'remember' and 'recall' by naming them as counterparts.

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

Usage Guidelines5/5

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

Explicitly states when to use the tool ('context is stale, task is done, clear sensitive data') and mentions pairing with 'remember' and 'recall', providing clear guidance on context and alternatives.

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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TDQS

A3.5/5.0
Disambiguation2/5

The FDA-specific tools are distinct, but they are mixed with many generic Pipeworx tools (e.g., ask_pipeworx variants, deep_research, entity_profile) that have overlapping purposes. This creates significant ambiguity for an agent trying to choose the right tool for FDA-related queries.

Naming Consistency2/5

Tool names follow two inconsistent patterns: FDA tools use 'fda_device_*' (consistent), while generic tools use various patterns like 'ask_pipeworx', 'deep_research', 'remember', etc. The mix of snake_case, camelCase, and descriptive phrases lacks coherence.

Tool Count2/5

With 37 tools, the count is high for what is intended as an FDA devices server. Only 6 tools are directly FDA-related; the rest are generic and dilute the purpose. The scope is mismatched, making the tool count inappropriate.

Completeness3/5

The FDA tools cover key areas: 510k search, adverse events, PMA, recalls, company profiles. However, the server is incomplete for its name because it lacks many tools that a comprehensive FDA devices server would have, and the generic tools don't fill those gaps.