Report an Adverse Event

Your safety is our priority. If you experience any adverse reaction or unexpected side effect from a Meo Nutrition product, we want to hear about it immediately.

How to Report an Adverse Event to Meo

Email us at support@meonutrition.com with the subject line "Adverse Event Report" so it routes directly to our Quality Assurance team. You can also reach us through the live chat widget at the bottom-right of any page on meonutrition.com — just lead with "I need to report an adverse event."

Please include:

• Your name and contact information
• The Meo Nutrition product (name + lot number from the bottle if available)
• Approximate dates of use
• Description of the reaction or side effect
• Whether you sought medical attention
• Any other relevant information

Response SLA: We acknowledge every adverse event report by email within 24 hours (typically much sooner during business hours). Our Quality Assurance team logs the event in our adverse event log per FDA requirements (DSHEA / Dietary Supplement and Nonprescription Drug Consumer Protection Act of 2006) and investigates promptly. Email is our official AE intake channel — please do not rely on social media DMs or third-party messaging for AE reports.

How to Report Directly to the FDA

You can also report adverse events directly to the FDA, and we encourage you to do so even if you've already contacted us. The FDA tracks patterns across the supplement industry and your report may help identify issues earlier.

• Phone: 1-800-FDA-1088 (1-800-332-1088)
• Online: FDA MedWatch reporting portal
• Mail: MedWatch, FDA, 5600 Fishers Lane, Rockville, MD 20857

Will Reporting Affect My Reviews or Account?

No. Reporting an adverse event does not:

• Prevent you from leaving a public product review about your overall experience
• Affect your ability to use your Meo Nutrition account or subscription
• Change our 90-day money-back guarantee for your purchase

Adverse event reports are handled separately from our review and refund processes. Both can run in parallel.

What We Do With Your Report

1. Acknowledge within 24 hours.
2. Log the event in our adverse event database (mandatory per FDA regulations).
3. Internal QA investigation: review the affected lot, manufacturing records, ingredient sources.
4. Report to FDA via MedWatch within FDA's required timeframe (15 business days for serious adverse events).
5. Follow up with you on findings and any corrective action.

Our Quality Person

Per FDA guidance, our Quality Assurance Lead is responsible for adverse event reporting compliance. All AE reports received at support@meonutrition.com are escalated to QA Lead within 1 business day of receipt.

Company & Mailing Information

Meo Nutrition LLC
1309 Coffeen Avenue, Suite 1200
Sheridan, Wyoming 82801
Email: support@meonutrition.com
Live chat: bottom-right widget on any page of meonutrition.com

This page is provided in compliance with FDA dietary supplement safety reporting requirements (21 CFR § 314.80, DSHEA, and the Dietary Supplement and Nonprescription Drug Consumer Protection Act of 2006). Last updated May 7, 2026.