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FD&C Act Section 417 • 24-Hour Deadline

Reportable Food Registry.

The 24-Hour Crisis Room. Automate your Reportable Food Registry (RFR) submissions to the FDA Safety Reporting Portal (SRP) before the clock runs out.

FDA Accepted
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24/7 Monitoring
RECALL ACTIVE
RECALL ACTIVE
RECALL ACTIVE
RFR Deadline
23:59:42
Event Classification
Type:Class I
Probability:Serious Adverse
CRITICAL ALERT: UNDECLARED ALLERGENS TOP RFR CAUSE - 24 HOUR DEADLINE
ENFORCEMENT: FAILURE TO FILE RFR REPORT WITHIN 24 HOURS = CRIMINAL LIABILITY
ALERT: LISTERIA MONOCYTOGENES POSITIVE - IMMEDIATE REPORTING REQUIRED
STATUS: SAFETY REPORTING PORTAL (SRP) ACTIVE - CHECK 2026 GUIDANCE
CRITICAL ALERT: UNDECLARED ALLERGENS TOP RFR CAUSE - 24 HOUR DEADLINE
ENFORCEMENT: FAILURE TO FILE RFR REPORT WITHIN 24 HOURS = CRIMINAL LIABILITY
ALERT: LISTERIA MONOCYTOGENES POSITIVE - IMMEDIATE REPORTING REQUIRED
STATUS: SAFETY REPORTING PORTAL (SRP) ACTIVE - CHECK 2026 GUIDANCE
CRITICAL ALERT: UNDECLARED ALLERGENS TOP RFR CAUSE - 24 HOUR DEADLINE
ENFORCEMENT: FAILURE TO FILE RFR REPORT WITHIN 24 HOURS = CRIMINAL LIABILITY
ALERT: LISTERIA MONOCYTOGENES POSITIVE - IMMEDIATE REPORTING REQUIRED
STATUS: SAFETY REPORTING PORTAL (SRP) ACTIVE - CHECK 2026 GUIDANCE
Assessment

Is it Reportable?

A food is “reportable” if there is a reasonable probability it will cause serious adverse health consequences or death (SAHCODHA). Class I recalls trigger mandatory RFR filing within 24 hours.

Undeclared Allergens
Pathogen Contamination
Step 1: Hazard Type
Biological
Chemical
Physical
Step 2: Severity
Reasonable Probability?
SAHCODHA Threshold
No
Yes
REPORTABLE
Submit to RFR within 24 hours. Notify supply chain.
START REPORT
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Assurentry Intake
Product InfoComplete
Contact DetailsComplete
Problem DescValidating...
FDA Safety Portal
SUBMITTED
FDA Portal Bridge

SRP Automation.

Navigating the FDA Safety Reporting Portal (SRP) during a crisis is prone to error. Our system auto-fills the required fields, validates mandatory data points, and submits directly via API.

Traceability

Immediate Notification.

The law requires you to notify “immediate previous sources” and “immediate subsequent recipients.” Our system blasts alerts to your supply chain automatically upon RFR submission.

Supplier
Reportable Event
Distributor
Retailer

Crisis Management Suite

Everything you need to manage a Class I recall situation.

24/7 Response

Our team is on standby to assist with hazard evaluation.

Amendment Tracking

Easily file follow-up reports as investigation continues.

Recall Strategy

Integration with recall management protocols.

Manual vs. Automated.

Speed reduces liability. Don't rely on manual data entry when 24 hours is the limit.

Comparison
FDA Portal (Direct)
Manual
Fastest
Assurentry
Automation
Submission Method
Direct SRP connection.
Manual Entry
Automated API
Data Validation
Prevents rejection.
None
Real-time Check
Notification
Suppliers & Consignees.
Manual Email
Auto-Broadcast
Record Retention
Audit-ready history.
Your Folder
Secure Vault
Amendment Support
Easy updates.
Difficult
1-Click

Don't miss the 24-hour window.

Seconds count when SAHCODHA is determined. Automate your RFR process today.

Frequently Asked Questions

Common questions about this regulatory requirement.

100% FDA Acceptance Guarantee

Secure Your Supply Chain.

Don't let a clerical error stop your shipment at the border. Join 2,800+ food companies who trust Assurentry for automated compliance.

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