HAZELNUT INTERNATIONAL delight COFFEE CREAMER
Reason The firm received complaints of spoilage and illness with the use of the products.
CINNABON CLASSIC CINNAMON ROLL INTERNATIONAL delight COFFEE CREAMER recall
Recalled by Danone Wave · Louisville, CO, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
The firm received complaints of spoilage and illness with the use of the products.
These are failures of the safety steps that keep food safe - cooking, pasteurising, keeping cold, sealing - even when no contaminant has yet been found. All processing & sanitation problems recalls.
What was recalled
CINNABON CLASSIC CINNAMON ROLL INTERNATIONAL delight COFFEE CREAMER 32 FL OZ (1 QT) 946 mL UPC 0 41271 01993 3 Distributed by: Danone US, LLC
Quantity: 7,747cs/6/32 fl oz bottles
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
BEST BY: 03 JUL 2025 51-4114 R-S
Where it was sold
Alabama Arkansas Colorado Connecticut Florida Georgia Illinois Indiana Kentucky Louisiana Maryland Maine Michigan Minnesota Missouri Mississippi North Carolina Nebraska New Hampshire New Jersey New Mexico New York Ohio Oklahoma Pennsylvania South Carolina Tennessee Texas Virginia Wisconsin Wyoming
FDA's distribution note: 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.
Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away.
- Recalling firm
- Danone Wave
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Feb 21, 2025
- In FDA report of
- Mar 19, 2025
- FDA recall number
- F-0625-2025 · event 96378
- Official record
- FDA enforcement report search
Also recalled with it (1 more product)
FDA files each product of one recall action separately; these share the same FDA event.
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