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FDA upgrades nationwide butter recall alert to a higher level

UNITED STATES, AUG 04 – Bunge North America voluntarily recalled 64,800 pounds of butter after FDA raised recall to Class II due to undeclared milk allergen risking reversible allergic reactions, no illnesses reported.

  • On July 14, 2025, Bunge North America Inc. initiated a recall of 64,800 pounds of NH European Style Butter Blend, which the FDA elevated to Class II on July 30 due to undeclared milk.
  • By omitting a major allergen, the butter label failed to declare milk, violating U.S. law that mandates identification of nine major food allergens.
  • The butter was sent to 12 distribution centers across the United States and one in the Dominican Republic, and is available at Amazon and Food Service Direct.
  • The FDA advises consumers to read the recall notice, verify product codes, and stop eating the affected butter if allergy symptoms occur, seeking emergency medication if needed.
  • Recalls for undeclared allergens are increasing nationwide, with allergy specialists noting a 300% to 400% rise in anaphylaxis rates in the United States.
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FDA upgrades butter recall alert to a higher level

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The product removed from the market is the NH European style butter manufactured by Bunge North America

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Newsweek broke the news in United States on Friday, August 1, 2025.
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