FDA Recall Alert: SiluetaYa Tejocote Root Dietary Supplement
Urgent safety notice: The U.S. Food & Drug Administration (FDA) has announced a voluntary recall of SiluetaYa Tejocote Root because laboratory tests identified the product as toxic yellow oleander (Thevetia peruviana). Stop using the supplement immediately and review the recall details below.
This guide explains the health risks, how to request a refund, and where to report any adverse reactions.
Why the SiluetaYa Tejocote Root Supplement Is Being Recalled
On October 27, 2023, SiluetaYa USA Inc. initiated the recall after FDA analysis confirmed that capsules advertised as genuine tejocote root were actually yellow oleander. Yellow oleander contains powerful cardiac glycosides that can trigger:
- Dangerous heart-rhythm changes (arrhythmia)
- Nausea, vomiting, and severe diarrhea
- Dizziness, confusion, or blurred vision
- Low blood pressure and, in extreme cases, cardiac arrest
Which SiluetaYa Products Are Impacted?
- Product name: SiluetaYa Tejocote Root
- Package size: 0.5-ounce (14 g) plastic container
- Distribution: Sold exclusively online through e-commerce marketplaces
- Recall scope: All lots and all UPC codes
What SiluetaYa Tejocote Root Consumers Should Do Now
- Immediately stop taking SiluetaYa Tejocote Root.
- Place the product in a sealed bag and return it to the seller for a full refund.
- Contact your healthcare provider if you have taken the supplement—even if you have no symptoms.
- Report adverse events to the FDA’s MedWatch program at MedWatch Online or 1-800-332-1088.
- For recall questions, email SiluetaYa at contacto@siluetaya.com (Mon–Fri, 10 a.m.–4 p.m. ET).
Health Risks of Yellow Oleander Contamination
Yellow oleander can interfere with the electrical signals in the heart and central nervous system. Even a small dose may cause:
- Palpitations or skipped heartbeats
- Severe abdominal pain and persistent vomiting
- Profuse sweating, weakness, or tremors
- Potentially fatal ventricular fibrillation in untreated cases
As of the recall date, no illnesses have been reported; however, the FDA urges consumers to act with caution due to the severity of potential effects.
Sources
Official Recall Images: SiluetaYa Tejocote Root
Frequently Asked Questions About the SiluetaYa Tejocote Root Recall
- Is every container of SiluetaYa Tejocote Root supplement recalled?
- Yes. The recall covers all lots, sizes, and UPC codes of SiluetaYa Tejocote Root sold online.
- Can I keep SiluetaYa Tejocote Root if I feel fine after taking it?
- No. Cardiac glycosides in yellow oleander can cause sudden toxicity. The FDA directs consumers to stop use and dispose of or return the product.
- How do I obtain a refund for my SiluetaYa Tejocote Root purchase?
- Contact the online retailer or marketplace where you bought the supplement. Provide proof of purchase and request a full refund in line with the recall instructions.
- What SiluetaYa Tejocote Root symptoms require immediate emergency care?
- Seek help for chest pain, heart palpitations, severe vomiting, dizziness, or fainting—especially within 24 hours of ingestion.
- Where was SiluetaYa Tejocote Root sold before the recall?
- The supplement was distributed exclusively through third-party e-commerce sites and was not available in brick-and-mortar stores.
- Does the SiluetaYa Tejocote Root recall include other SiluetaYa products?
- At this time, the FDA notice refers only to SiluetaYa Tejocote Root. No other SiluetaYa supplements are included.
- How do I report a side effect linked to SiluetaYa Tejocote Root to the FDA?
- File a report through the FDA’s MedWatch portal or call 1-800-332-1088. Include details such as the product name, symptoms, and date of consumption.