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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Food
Food & Beverages/Beverages

International Delight Peppermint Mocha Creamer Recalled for Mis-labeled Sugar

Agency Publication Date: October 28, 2024
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Summary

Danone US LLC is recalling approximately 1,799 cases of Home Alone International Delight Peppermint Mocha Zero Sugar creamer because the product actually contains sugar despite being labeled as a zero-sugar product. The recall affects 32-ounce plastic bottles sold in refrigerated sections. No incidents or injuries have been reported to date regarding this mis-labeling.

Risk

The product contains sugar but is labeled as 'Zero Sugar,' which poses a health risk to consumers who must strictly monitor their sugar intake for medical reasons, such as diabetes. Consuming unexpected sugar can lead to serious health complications for these individuals.

What You Should Do

  1. This recall affects 32oz plastic bottles of Home Alone International Delight Peppermint Mocha Zero Sugar creamer with the date code BEST BY 02.25.25.
  2. Return the product to the place of purchase for a full refund, throw it away, or contact the manufacturer for further instructions.
  3. Call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) if you have additional questions or need to report a concern.

Your Remedy Options

You have 2 options:

๐Ÿ’ฐOption 1: Full Refund
How to: Return the product to the place of purchase for a full refund, or contact the manufacturer or supplier for further instructions
๐Ÿ—‘๏ธOption 2: Dispose of Product
How to: Throw the product away.

Affected Products

Product: Home Alone International Delight Peppermint Mocha Zero Sugar (32oz)
Variants: Refrigerated, 6 bottles per case
Date Ranges: BEST BY 02.25.25

Recall #: F-0070-2025

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 95564
Status: Resolved
Manufacturer: DANONE US LLC
Manufactured In: United States
Units Affected: 1799 cases
Distributed To: Arkansas, Georgia, Illinois, Indiana, Iowa, Kentucky, Mississippi, New Mexico, Nebraska, Oklahoma, Tennessee, Texas, Wisconsin

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.