Food Recall Check
Class II · Moderate risk Ongoing Initiated Feb 21, 2025 (2 years ago)

HAZELNUT 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

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

Food: Juice & beverages

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: 02 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-0626-2025 · 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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