The U.S. Food and Drug Administration (FDA) has assigned a Class II risk warning to the recall of two sweetener products from NuNaturals, Inc. due to a mislabeling error that could pose a risk to individuals with certain allergies.
The Eugene, Oregon-based company initiated a voluntary recall on July 14 for specific lots of its Organic Pure Stevia and Pure Monk Fruit Sweetener. The products were found to have been packaged in the wrong bottles; those labeled as Pure Monk Fruit Sweetener actually contain stevia powder, while the bottles labeled Organic Pure Stevia contain monk fruit powder. The FDA classified the recall as Class II on August 1.
A Class II recall signifies a situation where using or being exposed to a product may cause temporary or medically reversible adverse health effects, or where the chance of serious health consequences is remote. The primary concern is for consumers with allergies. Stevia can cause reactions in people sensitive to ragweed and related plants, while monk fruit allergies, though rare, can also occur. Allergic reactions can range from mild symptoms like hives to severe, life-threatening anaphylaxis.
The recalled products were distributed nationwide to retailers and consumers. The affected items are:
- Pure Monk Fruit Sweetener: 0.71oz plastic bottle, UPC 7 39223 00187 6, Lot number 25104S, Best by April 2028. (Contains stevia)
- Organic Pure Stevia: 1oz plastic bottle, UPC 7 39223 00204 0, Lot number 25104S, Best by April 2028. (Contains monk fruit)
The FDA has confirmed the recall is ongoing. Consumers with allergies or sensitivities to stevia, ragweed, or monk fruit are advised not to consume the affected products.
