Eva Nutrition, Science of Alpha, Niwali, NWL Nutra: Tejocote Dietary Supplements — FDA announcement Apr 10, 2024

Published notice; closure not supplied

A company announcement posted by FDA. The listing date can differ from the original announcement date. The absence of a termination marker does not prove the recall is currently ongoing.

Source date Apr 10, 2024. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.

What the record says

Product
Tejocote Dietary Supplements
Reason
Product contains toxic yellow oleander.
Classification
Not supplied
Recalling firm
Global Mix, Inc.
Quantity
Not supplied
Agency-reported status
Company recall announcement
Source record identifier
ccc5edefbad9fd76

Open the official record

Lot and product identifiers

Label fieldDetails supplied by the agency
Lot, code or applicabilityRecalled Products include the following bearing below information. Product codes and expiration dates can be found on the bottom of the packaging.; Product Name | Serial No | Mfg Date | UPC Codes | Expiry Date; Eva Nutrition Mexican Tejocote root | 181121U | 08/01/2023 | | 06/2025; Science of Alpha Mexican Tejocote root | 181121U | 08/01/2023 | | 06/2025; NWL Nutra Mexican Tejocote root | 181121U | 08/01/2023 | | 06/2025; Niwali Mexican Tejocote root | 181121U | 08/01/2023 | | 06/2025

Match all identifying details in the current notice. A brand name alone is not enough.

Product tables from the announcement

These identifying details come from the company announcement posted by FDA. Check the current notice for revisions.

FDA company announcement, table 1
Product Name Serial No Mfg Date UPC Codes Expiry Date
Eva Nutrition Mexican Tejocote root 181121U 08/01/2023 06/2025
Science of Alpha Mexican Tejocote root 181121U 08/01/2023 06/2025
NWL Nutra Mexican Tejocote root 181121U 08/01/2023 06/2025
Niwali Mexican Tejocote root 181121U 08/01/2023 06/2025

Announcement retrieved Oct 1, 2026. Official announcement.

Distribution

The recalled products were distributed in the following states: Alabama, Alaska, California, Colorado, Connecticut, Delaware, Florida, Georgia, Hawaii, Idaho, Illinois, Iowa, Indiana, Kansas, Kentucky, Louisiana, Maryland, Massachusetts, Michigan, Minnesota, Mississippi, Missouri, Montana, Nebraska, Nevada, New Mexico, New Carolina, New York, New Jersey, North Dakota, Ohio, Oklahoma, Oregon, Pennsylvania, South Carolina, Tennessee, Texas, Utah, Virginia, Washington, West Virginia, Wisconsin, Wyoming through website. The recalled products were also sold via the below websites via courier direct delivery and mail order.

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

Dates in the source

Fda listing date
Apr 10, 2024
Company announcement date
Apr 5, 2024

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

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