Home Alone International Delight Peppermint Mocha Zero Sugar, 32oz plastic bottle, 6 bottles per case. Refrigerated.
Summary
The FDA issued a Class II for Home Alone International Delight Peppermint Mocha Zero Sugar, 32oz plastic bottl by DANONE US LLC. Reason: The International Delight Zero Sugar Peppermint Mocha is recalled because it was mis-labeled as zero sugar but it contains sugar..
Details
Source
Food Recall
External ID
F-0070-2025
Action Date
2024-11-06
Status
Terminated
Category
food
Product Description
Home Alone International Delight Peppermint Mocha Zero Sugar, 32oz plastic bottle, 6 bottles per case. Refrigerated.
Lot/Code Info: BEST BY 02.25.25
Quantity Affected: 1799 cases
Reason for Recall
The International Delight Zero Sugar Peppermint Mocha is recalled because it was mis-labeled as zero sugar but it contains sugar.
Distribution
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.
Type: Voluntary: Firm initiated
Recall Initiated: 2024-10-12
Company
Broomfield, CO
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 42 food recalls issued in the same week, part of 204 food-related FDA actions this month.
DANONE US LLC has 16 FDA actions in our database, including 16 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (DANONE US LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does DANONE US LLC have FDA actions?
DANONE US LLC has 16 FDA actions in our database, including 16 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0070-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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