FDA Issues Risk Warning for Nationwide Sweetener Recall

NuNaturals, Inc., based in Eugene, Oregon, issued a voluntary recall for specific lots of its Organic Pure Stevia and Pure Monk Fruit Sweetener after discovering a mislabeling error. The FDA subsequently issued a Class II risk warning, indicating a potential for temporary or medically reversible health consequences.

The affected products include Pure Monk Fruit Sweetener (UPC 7 39223 00187 6, Lot number: 25104S) and Organic Pure Stevia (UPC 7 39223 00204 0, Lot number: 25104S), both with a best-by date of April 2028. The mislabeling resulted in bottles labeled as Pure Monk Fruit Sweetener containing stevia powder, while the Organic Pure Stevia bottles contained monk fruit. These products were packaged in plastic bottles with white caps and distributed to retailers and consumers nationwide.

This recall is particularly important for individuals with allergies to ragweed, related plants, or monk fruit, as they may experience allergic reactions ranging from mild symptoms like hives and lip swelling to severe complications like anaphylaxis. Consumers are advised to check the labels and avoid consuming the affected products. The FDA emphasizes that individuals with food allergies should always read labels carefully to avoid foods they are allergic to.

Consumers with allergies or sensitivities to stevia, ragweed, related plants, and monk fruit should not consume the affected products and should discard them.

A Class II recall indicates that use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote.

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