Design Failure Mode and Effects Analysis (DFMEA) skill for systematic design risk identification
Scanned 9/2/2026
Install to Claude Code
npx -y skills add a5c-ai/babysitter --skill design-fmea-generator --agent claude-codeInstalls into .claude/skills of the current project.
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---
name: design-fmea-generator
description: Design Failure Mode and Effects Analysis (DFMEA) skill for systematic design risk identification
allowed-tools:
- Read
- Write
- Glob
- Grep
- Edit
- Bash
metadata:
specialization: biomedical-engineering
domain: science
category: Risk Management
skill-id: BME-SK-007
graph:
domains: [domain:biomedical-engineering]
skillAreas: [skill-area:statistical-analysis, skill-area:data-analysis, skill-area:compliance-automation]
workflows: [workflow:experiment-design, workflow:peer-review-cycle]
roles: [role:biomedical-engineer, role:research-engineer]
---
# Design FMEA Generator Skill
## Purpose
The Design FMEA Generator Skill facilitates systematic identification and evaluation of potential design failure modes for medical devices, supporting ISO 14971 risk management through structured DFMEA methodology.
## Capabilities
- DFMEA worksheet generation
- Failure mode brainstorming support
- Severity, Occurrence, Detection rating guidance
- RPN (Risk Priority Number) calculation
- Recommended action tracking
- Control plan linkage
- Failure mode categorization
- Root cause analysis templates
- Design mitigation recommendations
- DFMEA revision management
- Cross-reference to risk management file
## Usage Guidelines
### When to Use
- Initiating design risk analysis
- Evaluating design alternatives
- Supporting design reviews
- Updating risk assessments for design changes
### Prerequisites
- Design concept defined
- Functional requirements documented
- Intended use established
- Similar device failure data available
### Best Practices
- Conduct DFMEA early in design phase
- Include cross-functional team members
- Link to ISO 14971 risk management file
- Update with design iterations
## Process Integration
This skill integrates with the following processes:
- Medical Device Risk Management (ISO 14971)
- Design Control Process Implementation
- Design for Manufacturing and Assembly (DFMA)
- Verification and Validation Test Planning
## Dependencies
- AIAG FMEA templates
- ISO 14971 risk management framework
- Design documentation
- Historical failure data
- Industry failure mode databases
## Configuration
```yaml
design-fmea-generator:
rating-scales:
severity: 1-10
occurrence: 1-10
detection: 1-10
risk-thresholds:
rpn-action-limit: 100
severity-critical: 9
output-formats:
- worksheet
- summary-report
- action-tracker
```
## Output Artifacts
- DFMEA worksheets
- Failure mode catalogs
- RPN summary reports
- Recommended action lists
- Control plan inputs
- Design review inputs
- Risk management file updates
- Mitigation tracking logs
## Quality Criteria
- All design functions analyzed
- Failure modes comprehensively identified
- Ratings consistently applied
- High RPN items addressed
- Actions tracked to completion
- Linkage to ISO 14971 maintained
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