Every regulated industry has different databases, timelines, and compliance frameworks. SuperRecall.ai delivers purpose-built recall automation — not a generic one-size-fits-all tool.
Comprehensive compliance platforms for the most heavily regulated industries
ISO 13485 · FDA QMSR 2026 · EU MDR · Health Canada MDR
Automate UDI traceability, CAPA workflows, post-market surveillance, and Field Safety Corrective Actions — across FDA, Health Canada, EU MDR, and 15+ global jurisdictions. Always hit the 10-day reporting deadline.
FDA 21 CFR Part 211 · DSCSA · GxP Validated · ICH Q10 · EMA
Automate drug recall workflows, pharmacovigilance signal escalation, DSCSA batch traceability, and 15-day safety reports. GxP validated and 21 CFR Part 11 compliant — purpose-built for pharmaceutical manufacturers and CMOs.
FDA FSMA 204 · CFIA · USDA FSIS · Allergen Traceability
Automated monitoring of FDA, CFIA, and USDA FSIS databases. Track ingredients, manage allergens, ensure traceability. Reduce recall response time from 28 days to 3 days with AI-powered compliance automation.
Recall monitoring across 44+ global databases for every regulated sector
We support dozens of regulated industries. Our team can configure custom monitoring rules, regulatory database coverage, and compliance workflows tailored to your specific requirements.