FDA Recall United States Ongoing Historical recordClass II
DANONE WAVE
- Product
- CINNABON CLASSIC CINNAMON ROLL INTERNATIONAL delight COFFEE…
- Published
- March 19, 2025
- Distribution
- The product was shipped to the following…
DANONE WAVE Recall: The firm received complaints of spoilage and illness with the use of the products.
United States
OngoingClass II
- Company
- DANONE WAVE
- Product
- HAZELNUT INTERNATIONAL delight COFFEE CREAMER 32 FL OZ (1 QT…
- Recall date
- February 21, 2025
- Source
- FDA
Reason for recall
The firm received complaints of spoilage and illness with the use of the products.
- - Recall initiated
- - Reported by source
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| HAZELNUT INTERNATIONAL delight COFFEE CREAMER 32 FL OZ (1 QT) 32 FL OZ (1 QT) 946 mL UPC 0 41271 02565 2 Distributed by: Danone US, LLC | Not published in this source record | 4,762cs/6/32 fl oz bottles | BEST BY: 02 JUL 2025 51-4114 R-S |
Distribution
- The product was shipped to the following states: AL
- AR
- CO
- CT
- FL
- GA
- IL
- IN
- KY
- LA
- MD
- ME
- MI
- MN
- MO
- MS
- NC
- NE
- NH
- NJ
- NM
- NY
- OH
- OK
- PA
- SC
- TN
- TX
- VA
- WI & WY.
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0626-2025
- Event ID
- 96378
- Status
- Ongoing
- Classification
- Class II
- Company
- DANONE WAVE
- Product description
- HAZELNUT INTERNATIONAL delight COFFEE CREAMER 32 FL OZ (1 QT) 32 FL OZ (1 QT) 946 mL UPC 0 41271 02565 2 Distributed by: Danone US, LLC
- Quantity
- 4,762cs/6/32 fl oz bottles
- Reason
- The firm received complaints of spoilage and illness with the use of the products.
- Recall initiation date
- February 21, 2025
- Report date
- March 19, 2025
- Classification date
- Not published in this source record
- Termination date
- Not terminated as of this source record
- Distribution pattern
- The product was shipped to the following states: AL, AR, CO, CT, FL, GA, IL, IN, KY, LA, MD, ME, MI, MN, MO, MS, NC, NE, NH, NJ, NM, NY, OH, OK, PA, SC, TN, TX, VA, WI & WY.
- UPC, lot, and code information
- BEST BY: 02 JUL 2025 51-4114 R-S
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Letter
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Other products recalled under this same event
This recall shares FDA event ID 96378 with 1 other product entry in Public Health Trace.
Responsible company: DANONE WAVE
Other recalls from DANONE WAVE
FDA Recall United States Ongoing Historical recordClass II
DANONE WAVE
- Product
- CINNABON CLASSIC CINNAMON ROLL INTERNATIONAL delight COFFEE…
- Published
- March 19, 2025
- Distribution
- The product was shipped to the following…
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 |
|---|---|
| Alabama | 1 |
| Arkansas | 1 |
| Colorado | 1 |
| Connecticut | 1 |
| Florida | 1 |
| Georgia | 1 |
| Illinois | 1 |
| Indiana | 1 |
| Kentucky | 1 |
| Louisiana | 1 |
| Maryland | 1 |
| Maine | 1 |
| Michigan | 1 |
| Minnesota | 1 |
| Missouri | 1 |
| Mississippi | 1 |
| North Carolina | 1 |
| Nebraska | 1 |
| New Hampshire | 1 |
| New Jersey | 1 |
| New Mexico | 1 |
| New York | 1 |
| Ohio | 1 |
| Oklahoma | 1 |
| Pennsylvania | 1 |
| South Carolina | 1 |
| Tennessee | 1 |
| Texas | 1 |
| Virginia | 1 |
| Wisconsin | 1 |
| Wyoming | 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 "Ongoing." 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.
