tooluniverse-product-safety-surveillance

Warn

Audited by Snyk on Jun 13, 2026

Risk Level: MEDIUM
Full Analysis

MEDIUM W011: Third-party content exposure detected (indirect prompt injection risk).

  • Third-party content exposure detected (high risk: 0.85). The required runtime workflow calls openFDA endpoints (e.g., /drug/shortages.json, /device/recall.json, /device/event.json, /food/event.json, /animalandveterinary/event.json) and ingests the returned JSON fields into the agent’s LLM context; these records are authored by third parties (reporters/manufacturers/consumers) rather than the operating user, so they are outsider free-text/narratives (e.g., MAUDE mdr_text[].text) flowing into the model.

Issues (1)

W011
MEDIUM

Third-party content exposure detected (indirect prompt injection risk).

Audit Metadata
Risk Level
MEDIUM
Analyzed
Jun 13, 2026, 03:26 AM
Issues
1
Security Audit — snyk — tooluniverse-product-safety-surveillance