Danone Us Home Alone International Delight Peppermint Recall

Why it was recalled

The International Delight Zero Sugar Peppermint Mocha is recalled because it was mis-labeled as zero sugar but it contains sugar.

Product description

Home Alone International Delight Peppermint Mocha Zero Sugar, 32oz plastic bottle, 6 bottles per case. Refrigerated.

Lot numbers, UPCs & expiration codes

BEST BY 02.25.25

Where it was sold

Distributed directly in IA, IN, TN, and TX. Product was further distributed in AR, GA, IL, IN, IA, KY, MS, NM, NE, OK, TN, TX, and WI.

What to do if you have this product

Compare the brand, size, and lot/UPC codes on your package with the codes above.
If it matches, don't eat it. Return it to the store for a refund or throw it away.
Wash surfaces and containers that touched the product.
If you feel sick after eating it, contact your doctor. In an emergency call 911.

Recall details

Recall number: F-0070-2025
Classification: Class II
Status: Terminated
Recall initiated: Oct 12, 2024
FDA report date: Nov 6, 2024
Quantity: 1799 cases
Recall type: Voluntary: Firm initiated
Recalling firm: DANONE US LLC

Original FDA data

Every field from FDA enforcement report F-0070-2025, exactly as published.

Show all FDA fields

City: Broomfield
State: CO
Status: Terminated
Country: United States
Event ID: 95564
Address: 12002 Airport Way
Code information: BEST BY 02.25.25
Postal code: 80021-2546
Report date: Nov 6, 2024
Product type: Food
Recall number: F-0070-2025
Classification: Class II
Recalling firm: DANONE US LLC
Product quantity: 1799 cases
Termination date: Feb 12, 2025
Reason for recall: The International Delight Zero Sugar Peppermint Mocha is recalled because it was mis-labeled as zero sugar but it contains sugar.
Voluntary / mandated: Voluntary: Firm initiated
Product description: Home Alone International Delight Peppermint Mocha Zero Sugar, 32oz plastic bottle, 6 bottles per case. Refrigerated.
Distribution pattern: Distributed directly in IA, IN, TN, and TX. Product was further distributed in AR, GA, IL, IN, IA, KY, MS, NM, NE, OK, TN, TX, and WI.
Recall initiation date: Oct 12, 2024
Initial firm notification: E-Mail
Center classification date: Oct 28, 2024

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-0070-2025, published Nov 6, 2024. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: Oct 2, 2026. Content last changed: Oct 2, 2026.

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