FDA Recall United States Ongoing Historical recordClass I
World Green Nutrition Inc.
- Product
- ELV Control Herbal Supplement; 90 Capsules
- Published
- July 3, 2024
- Distribution
- Product is sold through authorized deale…
World Green Nutrition Inc. Recall: FDA analysis found product labeled as tejocote is actually contains yellow oleander, which is toxic to humans.
United States
TerminatedClass I
- Company
- World Green Nutrition Inc.
- Product
- ELV ALIPOTEC brand MEXICAN TEJOCOTE ROOT SUPPLEMENT PIECES (…
- Recall date
- January 6, 2024
- Terminated
- February 14, 2025
- Source
- FDA
Reason for recall
FDA analysis found product labeled as tejocote is actually contains yellow oleander, which is toxic to humans.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| ELV ALIPOTEC brand MEXICAN TEJOCOTE ROOT SUPPLEMENT PIECES (RAIZ DE TEJOCOTE MEXICANO SUPLEMENTO EN TROZOS), NET. WT, 0.3 0Z (7g) | Not published in this source record | 113,500 | LOT Expiration Date 090222 110424 070722 110424 150722N 120724 190722N 120724 150722N-1 120724 110522 120724 070722 120724 040722 120724 260522 120724 190722N-1 120724 150822 120724 160622 92324 030123 030728 150722N 030828 030123 030628 291122 030628 250123 030628 130123 030728 040722 031328 030123 031328 160622 031428 250123 031428 250123 031528 250123 032128 250123 032228 250123 032328 250123 032428 250123 032728 250123 032828 150722N 032828 160622 041928 260123D 041928 190722N 041928 250123 041828 140223 051228 030223 051228 010323 051528 190722N 051528 200722 051228 250123 051228 150722N 051228 020323 052328 260123D 052328 190722N 052428 260123D 071828 010323 071928 030223 071928 260123D 073128 260123D 080228 140223D 081528 |
Distribution
- TX
- CA
- AZ
- NC
- GA
- OR
- WA
- NM
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-1000-2024
- Event ID
- 93774
- Status
- Terminated
- Classification
- Class I
- Company
- World Green Nutrition Inc.
- Product description
- ELV ALIPOTEC brand MEXICAN TEJOCOTE ROOT SUPPLEMENT PIECES (RAIZ DE TEJOCOTE MEXICANO SUPLEMENTO EN TROZOS), NET. WT, 0.3 0Z (7g)
- Quantity
- 113,500
- Reason
- FDA analysis found product labeled as tejocote is actually contains yellow oleander, which is toxic to humans.
- Recall initiation date
- January 6, 2024
- Report date
- March 6, 2024
- Classification date
- Not published in this source record
- Termination date
- February 14, 2025
- Distribution pattern
- TX, CA, AZ, NC, GA, OR, WA, NM
- UPC, lot, and code information
- LOT Expiration Date 090222 110424 070722 110424 150722N 120724 190722N 120724 150722N-1 120724 110522 120724 070722 120724 040722 120724 260522 120724 190722N-1 120724 150822 120724 160622 92324 030123 030728 150722N 030828 030123 030628 291122 030628 250123 030628 130123 030728 040722 031328 030123 031328 160622 031428 250123 031428 250123 031528 250123 032128 250123 032228 250123 032328 250123 032428 250123 032728 250123 032828 150722N 032828 160622 041928 260123D 041928 190722N 041928 250123 041828 140223 051228 030223 051228 010323 051528 190722N 051528 200722 051228 250123 051228 150722N 051228 020323 052328 260123D 052328 190722N 052428 260123D 071828 010323 071928 030223 071928 260123D 073128 260123D 080228 140223D 081528
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- 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.
A map highlighting the states named in the source's distribution description.
Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.
| State | Distributed |
|---|---|
| Texas | 1 |
| California | 1 |
| Arizona | 1 |
| North Carolina | 1 |
| Georgia | 1 |
| Oregon | 1 |
| Washington | 1 |
| New Mexico | 1 |
States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.
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 "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.
