FDA Recall United States Terminated Historical recordClass II
DANONE US LLC
- Product
- YoCrunch Lowfat Yogurt with Toppers Two-product package. Co…
- Published
- July 23, 2025
- Distribution
- Nationwide
DANONE US LLC Recall: The International Delight Zero Sugar Peppermint Mocha is recalled because it was mis-labeled as zero sugar but it contains sugar.
United States
TerminatedClass II
- Company
- DANONE US LLC
- Product
- Home Alone International Delight Peppermint Mocha Zero Sugar…
- Recall date
- October 12, 2024
- Terminated
- February 12, 2025
- Source
- FDA
Reason for recall
The International Delight Zero Sugar Peppermint Mocha is recalled because it was mis-labeled as zero sugar but it contains sugar.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Home Alone International Delight Peppermint Mocha Zero Sugar, 32oz plastic bottle, 6 bottles per case. Refrigerated. | Not published in this source record | 1799 cases | BEST BY 02.25.25 |
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.
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0070-2025
- Event ID
- 95564
- Status
- Terminated
- Classification
- Class II
- Company
- DANONE US LLC
- Product description
- Home Alone International Delight Peppermint Mocha Zero Sugar, 32oz plastic bottle, 6 bottles per case. Refrigerated.
- Quantity
- 1799 cases
- Reason
- The International Delight Zero Sugar Peppermint Mocha is recalled because it was mis-labeled as zero sugar but it contains sugar.
- Recall initiation date
- October 12, 2024
- Report date
- November 6, 2024
- Classification date
- Not published in this source record
- Termination date
- February 12, 2025
- 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.
- UPC, lot, and code information
- BEST BY 02.25.25
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: DANONE US LLC
Other recalls from DANONE US LLC
FDA Recall United States Terminated Historical recordClass II
DANONE US LLC
- Product
- YoCrunch Lowfat Yogurt with Toppers. Two-product package.…
- Published
- July 23, 2025
- Distribution
- Nationwide
FDA Recall United States Terminated Historical recordClass II
DANONE US LLC
- Product
- YoCrunch Lowfat Yogurt with Toppers. Two-product packages.…
- Published
- July 23, 2025
- Distribution
- Nationwide
A map highlighting the states named in the source's distribution description.
Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.
| State | Distributed |
|---|---|
| Iowa | 1 |
| Indiana | 1 |
| Tennessee | 1 |
| Texas | 1 |
| Arkansas | 1 |
| Georgia | 1 |
| Illinois | 1 |
| Kentucky | 1 |
| Mississippi | 1 |
| New Mexico | 1 |
| Nebraska | 1 |
| Oklahoma | 1 |
| Wisconsin | 1 |
States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.
Where this information comes from
View FDA enforcement record -- the specific openFDA record this summary was built from.
No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information.
Technical source data
View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
Frequently asked questions
What does a Class II mean?
A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.
Is this recall still active?
According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
What should I do if I have this product?
Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.
Where can I find more official information?
The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.
This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.
