A recall of two plant-based sweetener products from NuNaturals Inc. was given the second-highest risk warning by the Food and Drug Administration, according to two notices published by the agency.
A mix-up of the labeling showed the stevia bottles were filled with the monk fruit sweetener, while the monk fruit sweetener was filled with stevia. The company initiated the recall last month, but the FDA on Aug. 1 said that has a Class II risk.
NuNaturals recalled 78 bottles of its Organic Pure Stevia and 78 bottles of its Pure Monk Fruit Sweetener, with both products being sold in plastic bottles with white caps, according to the FDA notices.
The recall impacts products that were sold nationwide. The FDA and NuNaturals, in the notices, did not say what stores may have been impacted.
Impacted Organic Pure Stevia bottles have the UPC 7 39223 00204 0 and lot number 25104S, according to the notice. And recalled Pure Monk Fruit Sweetener bottles have the UPC 7 39223 00187 and lot number 25104S.
It's also not clear whether any adverse events or injuries were reported in association with the recalls.
A Class II, or the second-highest risk level out of three levels, means that there is a "situation in which 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," the FDA says on its website.
This month's NuNaturals recall update is the latest in a series of mislabeling incidents that have prompted recalls of other products.
