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Popular Sweetener Recalled Nationwide as FDA Warns of Label Mix-Up

UNITED STATES, AUG 7 – NuNaturals recalled 156 bottles of sweeteners after a labeling error posed allergic risks to ragweed-sensitive consumers, with the FDA classifying it as a Class II health hazard.

  • On July 14, NuNaturals voluntarily recalled 156 bottles nationwide due to a labeling error that caused stevia and monk fruit sweeteners to be incorrectly packaged and distributed.
  • The recall was initiated due to a labeling error where bottles marked as Stevia were filled with Monk Fruit powder and those labeled as Monk Fruit contained Stevia, posing allergen concerns for individuals with sensitivities.
  • A total of 78 bottles each of the Monk Fruit and Stevia sweeteners, identified by specific UPC codes and lot numbers, were made available to retailers throughout the United States.
  • On August 1, the FDA raised the recall status to Class II, signaling that exposure to the affected products could result in temporary or reversible health effects.
  • The recall remains ongoing and advises consumers not to use the affected products, highlighting the importance of caution for people allergic to stevia, ragweed-related plants, or monk fruit.
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Health broke the news in United States on Thursday, August 7, 2025.
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