ELV ALIPOTEC brand MEXICAN TEJOCOTE ROOT SUPPLEMENT PIECES (RAIZ DE TEJOCOTE MEXICANO SUPLEMENTO EN TROZOS), NET. WT,... — FDA record F-1000-2024

Reported terminated

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Jan 6, 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
ELV ALIPOTEC brand MEXICAN TEJOCOTE ROOT SUPPLEMENT PIECES (RAIZ DE TEJOCOTE MEXICANO SUPLEMENTO EN TROZOS), NET. WT, 0.3 0Z (7g)
Reason
FDA analysis found product labeled as tejocote is actually contains yellow oleander, which is toxic to humans.
Classification
Class I
Recalling firm
World Green Nutrition Inc.
Quantity
113,500
Agency-reported status
Terminated
Source record identifier
F-1000-2024

Open the official record

What the recall classes mean. Classification is an agency assessment, not individual medical advice.

Lot and product identifiers

Label fieldDetails supplied by the agency
Lot, code or applicabilityLOT 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

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

Distribution

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

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

Dates in the source

Report date
Mar 6, 2024
Recall initiation date
Jan 6, 2024
Center classification date
Feb 29, 2024
Termination date
Feb 14, 2025

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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