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NuNaturals Inc Recall: Product is Monk Fruit powder but bottle was mis-labeled as Organic Pure Stevia.

United States

TerminatedClass II

Company
NuNaturals Inc
Product
Organic Pure Stevia, net wt. 1oz. UPC 7 39223 00204 0. Produ…
Recall date
July 14, 2025
Terminated
November 21, 2025
Source
FDA

Reason for recall

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

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
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. Not published in this source record 78 bottles (total) 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

Distribution

  • Nationwide

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
H-0380-2025
Event ID
97252
Status
Terminated
Classification
Class II
Company
NuNaturals Inc
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.
Quantity
78 bottles (total)
Reason
Product is Monk Fruit powder but bottle was mis-labeled as Organic Pure Stevia.
Recall initiation date
July 14, 2025
Report date
August 6, 2025
Classification date
Not published in this source record
Termination date
November 21, 2025
Distribution pattern
Nationwide
UPC, lot, and code information
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
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Other products recalled under this same event

This recall shares FDA event ID 97252 with 1 other product entry in Public Health Trace.

FDA Recall United States Terminated Historical recordClass II

NuNaturals Inc

Product
Pure Monk Fruit Sweetener, net wt. 0.71oz. UPC 7 39223 00187…
Published
August 6, 2025
Distribution
Nationwide

View recall →

Responsible company: NuNaturals Inc

Other recalls from NuNaturals Inc

FDA Recall United States Terminated Historical recordClass II

NuNaturals Inc

Product
Pure Monk Fruit Sweetener, net wt. 0.71oz. UPC 7 39223 00187…
Published
August 6, 2025
Distribution
Nationwide

View recall →

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace:

Frequently asked questions

What does a Class II mean?

A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.