FDA Recall United States Terminated Historical recordClass I
World Green Nutrition Inc.
- Product
- ELV ALIPOTEC brand MEXICAN TEJOCOTE ROOT SUPPLEMENT PIECES (…
- Published
- March 6, 2024
- Distribution
- Multiple states
World Green Nutrition Inc. Recall: FDA Analysis found product labeled as tejocote is actually yellow oleander, which is toxic to humans.
United States
OngoingClass I
- Company
- World Green Nutrition Inc.
- Product
- ELV Control Herbal Supplement; 90 Capsules
- Recall date
- April 3, 2024
- Source
- FDA
Reason for recall
FDA Analysis found product labeled as tejocote is actually yellow oleander, which is toxic to humans.
- - Recall initiated
- - Reported by source
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| ELV Control Herbal Supplement; 90 Capsules | Not published in this source record | 20,092 units | N1082701 050328; GESPM240622 071324; GESPM300; 622 071324; GESPM050722 071324; 190620230009B 061928; 190620231573678B 062828280620231; 573678BA 062828 |
Distribution
- 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.
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-1391-2024
- Event ID
- 94346
- Status
- Ongoing
- Classification
- Class I
- Company
- World Green Nutrition Inc.
- Product description
- ELV Control Herbal Supplement; 90 Capsules
- Quantity
- 20,092 units
- Reason
- FDA Analysis found product labeled as tejocote is actually yellow oleander, which is toxic to humans.
- Recall initiation date
- April 3, 2024
- Report date
- July 3, 2024
- Classification date
- Not published in this source record
- Termination date
- Not terminated as of this source record
- Distribution pattern
- 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.
- UPC, lot, and code information
- N1082701 050328; GESPM240622 071324; GESPM300; 622 071324; GESPM050722 071324; 190620230009B 061928; 190620231573678B 062828280620231; 573678BA 062828
- 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
Responsible company: World Green Nutrition Inc.
Other recalls from World Green Nutrition Inc.
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 I mean?
A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.
Is this recall still active?
According to FDA, this recall's status is "Ongoing." 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?
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