Organic Pure Stevia
Reason Product is Monk Fruit powder but bottle was mis-labeled as Organic Pure Stevia.
Pure Monk Fruit Sweetener recall
Recalled by NuNaturals Inc · Eugene, OR, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Product is Stevia powder but bottle was mis-labeled as Pure Monk Fruit Sweetener.
A label that does not match the product can hide an ingredient someone must avoid, or show a wrong use-by date. All labeling errors recalls.
What was recalled
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.
Quantity: 78 bottles (total)
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
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
Where it was sold
Nationwide.
FDA's distribution note: Nationwide
Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- NuNaturals Inc
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Jul 14, 2025
- In FDA report of
- Aug 6, 2025
- Terminated
- Nov 21, 2025
- FDA recall number
- H-0381-2025 · event 97252
- Official record
- FDA enforcement report search
Also recalled with it (1 more product)
FDA files each product of one recall action separately; these share the same FDA event.