Food recall
World Green Nutrition Inc. recall: ELV Control Herbal Supplement
World Green Nutrition Inc., of San Antonio, TX, recalled ELV Control Herbal Supplement. The FDA's reason: “FDA Analysis found product labeled as tejocote is actually yellow oleander, which is toxic to humans.” The FDA classified it Class I: it could cause serious harm or death. The company began the recall voluntarily on April 3, 2024, and the FDA first listed it in its Enforcement Report of July 3, 2024. The recall is still going on.
How serious
Class I
It could cause serious harm or death
Why
Lead or other chemicals
Status
Ongoing
The recall
- Company
- World Green Nutrition Inc. (San Antonio, TX)
- Reason, in FDA's words
- “FDA Analysis found product labeled as tejocote is actually yellow oleander, which is toxic to humans.”
- Where it was sold
- Product is sold through authorized dealers and E-commerce throughout the USA and Mexico, While the products, Elv Control Herbal Supplement and Mexican Tejocote Root Supplement Pieces (Raiz de Tejocote Mexicano Suplemento en Trozos), were intended to be distributed only through authorized distributors, it is possible that these products were purchased and further distributed via e-commerce platforms and/ or physical stores.
- Recall began
- , by the company
- FDA classified it
- First in an FDA Enforcement Report
- FDA event number
- 94346
The product recalled
As the FDA describes them, with the codes that tell whether a package is part of the recall.
-
F-1391-2024 Class I
ELV Control Herbal Supplement; 90 Capsules
Codes: N1082701 050328; GESPM240622 071324; GESPM300; 622 071324; GESPM050722 071324; 190620230009B 061928; 190620231573678B 062828280620231; 573678BA 062828
Quantity: 20,092 units
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Source and notes
U.S. Food and Drug Administration, Enforcement Reports (openFDA food recall data) (Public domain (U.S. government work); source U.S. Food and Drug Administration, openFDA), data as of July 3, 2024.
Each week the FDA lists the recalls it has classified in its Enforcement Report, often weeks after the company announced the recall, so a month with five weekly reports tends to count more. Each recall counts once, however many products it covers, in the month FDA first listed it. Class I means the food could cause serious harm or death, Class II temporary or minor harm, and Class III is unlikely to harm anyone. Meat, poultry and most egg products are recalled by the U.S. Department of Agriculture, not the FDA, and aren't included. For what to do with a recalled product, see the FDA's recalls page.