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Natural Organics, Inc. Recall: Contains undeclared wheat (gluten) in product labeled "gluten free"

United States

TerminatedClass II

Company
Natural Organics, Inc.
Product
Keto Living Sugar Control
Recall date
May 3, 2022
Terminated
April 30, 2024
Source
FDA

Reason for recall

Contains undeclared wheat (gluten) in product labeled "gluten free"

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
Keto Living Sugar Control Not published in this source record 4,650 bottles Product Code 82004 with lot codes 1362073 and 1365200 Product Code: Ue82004 with lot codes 1361754 and 1364325

Distribution

  • Nationwide; United Arab Emirates
  • Kenya
  • Spain
  • Trinidad
  • and the United Kingdom.

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-1101-2022
Event ID
90131
Status
Terminated
Classification
Class II
Company
Natural Organics, Inc.
Product description
Keto Living Sugar Control
Quantity
4,650 bottles
Reason
Contains undeclared wheat (gluten) in product labeled "gluten free"
Recall initiation date
May 3, 2022
Report date
June 8, 2022
Classification date
Not published in this source record
Termination date
April 30, 2024
Distribution pattern
Nationwide; United Arab Emirates, Kenya, Spain, Trinidad, and the United Kingdom.
UPC, lot, and code information
Product Code 82004 with lot codes 1362073 and 1365200 Product Code: Ue82004 with lot codes 1361754 and 1364325
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
E-Mail
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Responsible company: Natural Organics, Inc.

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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.