HAZELNUT INTERNATIONAL delight COFFEE CREAMER 32 FL OZ (1 QT) 32 FL OZ (1 QT) 946 mL UPC 0 41271 02565 2 Distributed by:
Summary
The FDA issued a Class II for HAZELNUT INTERNATIONAL delight COFFEE CREAMER 32 FL OZ (1 QT) 32 FL OZ (1 QT) 94 by DANONE WAVE. Reason: The firm received complaints of spoilage and illness with the use of the products..
Details
Source
Food Recall
External ID
F-0626-2025
Action Date
2025-03-19
Status
Ongoing
Category
food
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
Lot/Code Info: BEST BY: 02 JUL 2025 51-4114 R-S
Quantity Affected: 4,762cs/6/32 fl oz bottles
Reason for Recall
The firm received complaints of spoilage and illness with the use of the products.
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.
Type: Voluntary: Firm initiated
Recall Initiated: 2025-02-21
Company
Louisville, 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 55 food recalls issued in the same week, part of 204 food-related FDA actions this month.
DANONE WAVE has 2 FDA actions in our database, including 2 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 WAVE) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does DANONE WAVE have FDA actions?
DANONE WAVE has 2 FDA actions in our database, including 2 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0626-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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