World Green Nutrition Inc. recalls ELV ALIPOTEC Mexican Tejocote Root Supplement Pieces due to FDA finding toxic yellow oleander in product. Stop using immediately.
FDA analysis found product labeled as tejocote is actually contains yellow oleander, which is toxic to humans.
World Green Nutrition Inc. is recalling ELV ALIPOTEC Mexican Tejocote Root Supplement Pieces because FDA analysis found the product contains yellow oleander, which is toxic to humans. This recall is critical as ingestion of yellow oleander can cause serious health risks.
The product is labeled as tejocote but contains yellow oleander, a plant toxic to humans. Ingestion of yellow oleander can cause severe health issues, including nausea, vomiting, and potentially life-threatening reactions.
Anyone who purchased ELV ALIPOTEC Mexican Tejocote Root Supplement Pieces from any retailer. People who consume the supplement regularly are at highest risk due to the toxic yellow oleander content.
Look for ELV ALIPOTEC brand Mexican Tejocote Root Supplement Pieces (RAIZ DE TEJOCOTE MEXICANO SUPLEMENTO EN TROZOS) with net weight 0.3 oz (7g). The product has specific lot numbers and expiration dates listed in the recall notice.
Immediately stop using the ELV ALIPOTEC Mexican Tejocote Root Supplement Pieces if you have them.
FDA analysis found the product labeled as tejocote contains yellow oleander, which is toxic to humans.
Stop using the product immediately and contact the manufacturer for further instructions.
Yes, ingestion of yellow oleander can cause serious health issues, including nausea, vomiting, and potentially life-threatening reactions.
We’ve drafted a message you can send ELV ALIPOTEC to request your refund or repair — edit it as you like.
Subject: Recall F-1000-2024 — ELV ALIPOTEC ELV ALIPOTEC Hello, I own a ELV ALIPOTEC that is covered by recall F-1000-2024 from ELV ALIPOTEC. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
