What Happened
On July 14, 2025, Bunge North America Inc. voluntarily recalled approximately 64,800 pounds of its NH European Style Butter Blend after discovering that milk, a major allergen, was not properly declared on the label. The U.S. Food and Drug Administration (FDA) later elevated the recall to a Class II recall on July 30, 2025, indicating that consumption could lead to temporary or medically reversible health consequences, with a remote chance of serious harm.
Why It Matters for Families
This recall affects households with individuals who have milk allergies. An undeclared allergen can trigger reactions ranging from mild symptoms like rashes or gastrointestinal discomfort to severe anaphylaxis, which can be life-threatening. Parents should be aware that milk is one of the nine major food allergens protected by law.
Identifying the Recalled Product
- Product: NH European Style Butter Blend
- Lot Code: 5064036503
- UPC: 1 00 78684 73961 2
- Packaging: White paperboard cases, 36 one-pound blocks per case
- Number of Cases Recalled: 1,800 (totaling 64,800 pounds)
The recalled butter was distributed to 12 distribution centers across the United States and one center in the Dominican Republic, with sales through foodservice channels and online retailers.
Steps for Parents
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If anyone in your household has a milk allergy:
- Do not use the product.
- Contact the seller or distributor for a refund or disposal instructions.
- If accidental exposure occurs, follow your allergy action plan, including using epinephrine if prescribed, and seek medical care immediately.
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If your family does not have a milk allergy:
- The recall is due to labeling, not contamination; however, you may return the product for a refund if it matches the codes above.
Protecting Your Child’s Environment
Inform all caregivers—such as school cafeterias, daycare providers, and family members—about this recall. Encourage them to check ingredient labels and lot codes on bulk butter products used in meal preparation.
Understanding Recall Classifications
A Class II recall means the product may cause temporary or medically reversible health issues. The probability of serious adverse consequences is remote.
