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Food FDA Class II Terminated Mislabeling

Pure Monk Fruit Sweetener, net wt. 0.71oz. UPC 7 39223 00187 6. Product is packaged in a plastic bottle with white cap. Ingredient: Monk Fruit (Luo Han Guo) Extract. Monk Fruit is so much sweeter than sugar, a pinch is all you need. Suggested Use: Add to sweeten your food or beverage. 1/64 tsp (a

NuNaturals Inc Published Aug 6, 2025

Risk level

Class II

May cause a temporary or reversible health problem; slight chance of serious harm.

Severity score 55/100

What should you do?

  • Check whether you have this product, using the lot codes, UPCs, and dates listed below.
  • Do not eat, serve, or sell the affected product.
  • Return it to the place of purchase for a refund, or throw it away in a sealed bag so people and animals can’t get to it.
  • Contact NuNaturals Inc or your place of purchase with questions, and see the source record below for full details.
Reason for recall

Product is Stevia powder but bottle was mis-labeled as Pure Monk Fruit Sweetener.

Affected products (1)

Pure Monk Fruit Sweetener, net wt. 0.71oz. UPC 7 39223 00187 6. Product is packaged in a plastic bottle with white cap. Ingredient: Monk Fruit (Luo Han Guo) Extract. Monk Fruit is so much sweeter than sugar, a pinch is all you need. Suggested Use: Add to sweeten your food or beverage. 1/64 tsp (a pinch) tastes as sweet as 1 tsp of sugar. Distributed by: NuNaturals, Inc. Eugene, OR 97402.

78 bottles (total)

Lot codes: Number
Code info: Best By 4/28 25104S Code Explained: Best By: April 2028. Lot Number: 25104S Represents date of production: YYDDD[S] YY 25 = 2025 Julian day = 104 [S] = 1 digit alpha suffix

Affected areas

Nationwide

Timeline

  1. Initiated
    Jul 14, 2025
  2. Published
    Aug 6, 2025
  3. Terminated
    Nov 21, 2025
Recall number
H-0381-2025
Agency
U.S. Food and Drug Administration
Country
US
Source data (openFDA JSON) About FDA enforcement reports

FDA records come from the openFDA food enforcement-report dataset — the agency's full weekly enforcement list. Most entries are not issued as consumer press releases, so they won't appear on fda.gov/recalls or in a web search. The source record link above resolves this exact recall by its number.