Organic Pure Stevia, net wt. 1oz. UPC 7 39223 00204 0. Product is packaged in a plastic bottle with white cap. Ingredie
Summary
The FDA issued a Class II for Organic Pure Stevia, net wt. 1oz. UPC 7 39223 00204 0. Product is packaged in a by NuNaturals Inc. Reason: Product is Monk Fruit powder but bottle was mis-labeled as Organic Pure Stevia..
Details
Source
Food Recall
External ID
H-0380-2025
Action Date
2025-08-06
Status
Terminated
Category
food
Product Description
Organic Pure Stevia, net wt. 1oz. UPC 7 39223 00204 0. Product is packaged in a plastic bottle with white cap. Ingredient: Organic Stevia Extract. Sprinkle a pinch for the perfect sweetness. Suggested Use: 1/64 tsp tastes as sweet as 1 tsp of sugar. Distributed by: NuNaturals, Inc. Eugene, OR 97402.
Lot/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
Quantity Affected: 78 bottles (total)
Reason for Recall
Product is Monk Fruit powder but bottle was mis-labeled as Organic Pure Stevia.
Distribution
Nationwide
Type: Voluntary: Firm initiated
Recall Initiated: 2025-07-14
Company
Eugene, OR
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 85 food recalls issued in the same week, part of 204 food-related FDA actions this month.
NuNaturals Inc has 2 FDA actions in our database, including 2 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (NuNaturals Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does NuNaturals Inc have FDA actions?
NuNaturals Inc has 2 FDA actions in our database, including 2 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0380-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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