Nationwide Butter Recall: Undeclared Allergen Prompts FDA Risk Warning

Why this matters: For individuals with milk allergies, consuming this butter blend could lead to adverse health reactions. The recall underscores the importance of clear allergen labeling to protect consumer health.

Bunge North America Inc., based in Missouri, issued a voluntary recall of its NH European Style Butter Blend because milk may not have been listed on the product's label. The FDA classified this as a Class II recall, meaning that exposure to the product may cause temporary or medically reversible health issues. The product, packaged in white paperboard cases with 36 blocks per case, was shipped to 12 distribution centers across the U.S. and one in the Dominican Republic.

The affected product details:

This recall highlights the critical role of accurate allergen labeling in food products. Milk allergies are common, especially in children, and can cause reactions ranging from hives to life-threatening anaphylaxis. Consumers with milk allergies should be vigilant about checking product labels and avoiding the recalled butter blend.

The Healthy by Reader's Digest reports that the recall was initiated on July 14 and classified as a Class II event on July 30.

If you have a milk allergy, discard the product immediately or return it to the place of purchase.

Symptoms can range from mild issues like hives and lip swelling to severe reactions like anaphylaxis, including wheezing, vomiting, and digestive problems.

The butter was sent to 12 distribution centers located throughout the U.S., as well as one distribution center in the Dominican Republic.

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