Class ITerminated in FDA datasetRecall initiated Jan 6, 2024

ELV ALIPOTEC brand MEXICAN TEJOCOTE ROOT SUPPLEMENT PIECES (RAIZ DE TEJOCOTE MEXICANO…

Recalling firm: World Green Nutrition Inc.

Why it was recalled

FDA analysis found product labeled as tejocote is actually contains yellow oleander, which is toxic to humans.

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Feb 14, 2025.

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Compare the exact product and package details with the label you have.

ProductELV ALIPOTEC brand MEXICAN TEJOCOTE ROOT SUPPLEMENT PIECES (RAIZ DE TEJOCOTE MEXICANO SUPLEMENTO EN TROZOS), NET. WT, 0.3 0Z (7g)
Package size7g

FDA 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

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Full FDA record and distribution details

Original product description

ELV ALIPOTEC brand MEXICAN TEJOCOTE ROOT SUPPLEMENT PIECES (RAIZ DE TEJOCOTE MEXICANO SUPLEMENTO EN TROZOS), NET. WT, 0.3 0Z (7g)

Original FDA recall reason

FDA analysis found product labeled as tejocote is actually contains yellow oleander, which is toxic to humans.

Recall details

Recall number
F-1000-2024
Event ID
93774
FDA status
Terminated
Initiated
Jan 6, 2024
Reported
Mar 6, 2024
Classified
Feb 29, 2024
Terminated
Feb 14, 2025
Quantity
113,500
Location
San Antonio, TX, United States
Initiation type
Voluntary: Firm initiated
Notification
E-Mail

Where it was distributed

TX, CA, AZ, NC, GA, OR, WA, NM

FDA source record · F-1000-2024

Data updated September 16, 2026. View official FDA data ↗

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