NH EUROPEAN STYLE BUTTER BLEND, BUNGE, NET WT 1 LB, MFD IN USA BY: Bunge Oils, Chesterfield, MO 63017, packed in white p
Summary
The FDA issued a Class II for NH EUROPEAN STYLE BUTTER BLEND, BUNGE, NET WT 1 LB, MFD IN USA BY: Bunge Oils, C by BUNGE NORTH AMERICA INC. Reason: allergen labeling - undeclared milk.
Details
Source
Food Recall
External ID
H-0354-2025
Action Date
2025-08-06
Status
Terminated
Category
food
Product Description
NH EUROPEAN STYLE BUTTER BLEND, BUNGE, NET WT 1 LB, MFD IN USA BY: Bunge Oils, Chesterfield, MO 63017, packed in white paperboard cases (36 blocks to a case) OW NH EURO BLEND SOLIDS 2015918
Lot/Code Info: Product 5023937, UPC 1 00 78684 73961 2, Lot code: 5064036503
Quantity Affected: 64,800 pounds (1,800 cases)
Reason for Recall
allergen labeling - undeclared milk
Distribution
12 distribution centers located throughout the U.S. 1 distribution center located in Dominican Republic
Type: Voluntary: Firm initiated
Recall Initiated: 2025-07-14
Company
Chesterfield, MO
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 85 food recalls issued in the same week, part of 204 food-related FDA actions this month.
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 (BUNGE NORTH AMERICA INC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does BUNGE NORTH AMERICA INC have FDA actions?
This is the only FDA action we have on record for BUNGE NORTH AMERICA INC in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0354-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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