Class I U.S. Food and Drug Administration

SiluetaYa Tejocote Root dietary supplement recall: Product contains yellow oleander

Recall published 12 months ago

Product contains yellow oleander

SiluetaYa Dietary supplements — recalled dietary supplements
Photo published by U.S. Food and Drug Administration with the recall notice.

The hazard: Drug safety concern

A problem with this medicine prompted the recall. With prescriptions, the first move is a conversation rather than a decision.

What the notice says: Ingestion of yellow oleander can cause severe or even fatal neurological, gastrointestinal, and cardiovascular adverse health effects.

Why it matters: The FDA recorded an enforcement action against this product. The classification and the summary above describe how serious the agency considers it.

Recall details

Recall number
H-0647-2026
Published
November 4, 2025
Risk level
Class I
Status
Ongoing
Issued by
U.S. Food and Drug Administration
Brand
SiluetaYa
Product type
Dietary supplements
Units affected
40 units
Distribution
Arizona, California, New Mexico, New York, Texas, Utah
Lot / code info
Lot: US1220, Expiration Date: 06/2027
UPC codes
7500464462411
Reports of harm
No illnesses have been reported to date.

Products covered by this recall

Tejocote Root dietary supplement

What the company announced

SiluetaYa is recalling its tejocote root because FDA analysis has determined that the products appear to be Thevetia peruviana, or yellow oleander. All parts of the yellow oleander plant are known to contain cardiac glycosides, which are highly toxic to humans and animals. Ingestion of yellow oleander can cause severe or even fatal neurological, gastrointestinal, and cardiovascular adverse health effects. Symptoms may include nausea, vomiting, dizziness, diarrhea, abdominal pain, changes in heart rhythm, arrhythmia, and more.

The tejocote root was distributed online.

The product comes in an 8-ounce container.

No illnesses have been reported to date.

The recall was the result of sampling conducted by the FDA.

Consumers who purchased tejocote root from the SiluetaYa line are advised not to consume it and to return it to the place of purchase for a full refund. Consumers with questions can contact the company at [email protected] Monday through Friday from 10:00 am to 4:00 pm Eastern Time.

Reproduced from the company announcement posted on fda.gov. Links and contact forms in the original are not repeated here; the official notice below has them.

Check your product

The notice names 5 codes you can read straight off the package. Type the one printed on yours and the list below narrows to it.

UPC / barcode

Read the twelve digits under the barcode on the package.

  • 7500464462411

Lot or batch code

Usually ink-stamped near the seam, the cap or the bottom of the pack.

  • US1220

Best-by / use-by date

Printed beside the lot code, not on the price sticker.

  • 06
  • 2027

Package size

Match the net weight or the piece count on the front of the pack.

  • 8 ounce

Codes are lifted verbatim from the FDA — Company recall announcements notice. A code that is missing here may still be covered — the official notice is the complete list.

What to do about Drug safety

SiluetaYa — A problem with this medicine prompted the recall. With prescriptions, the first move is a conversation rather than a decision.

  1. Check the lot number on your pack against the codes listed above.
  2. Keep the carton; the lot number is often printed only on the outer pack.
  3. Report side effects you think the product caused to FDA MedWatch.
  4. Do not stop a prescribed medicine on your own — speak to your prescriber or pharmacist first.

Getting a replacement supply

Do not let a refund question interrupt your treatment. Deal with the supply first and the money second.

  • Call the pharmacy before you run low. They can see which lot they dispensed to you and will usually swap it the same day.
  • Insurers do not normally count a recall replacement against a refill limit. If one is refused, ask the pharmacist to call it through as a recall override.
  • Over-the-counter products are refunded at the till like any other purchase; the recall notice on your phone is enough to explain the return.
  • If the manufacturer runs a direct reimbursement form, it will be linked from the official notice on this page.

Remedy named in the notice: Consumers who purchased tejocote root from the SiluetaYa line are advised not to consume it and to return it to the place of purchase for a full refund.

Company contact: SiluetaYa — Consumers: [email protected]

The official notice

This page summarises a notice published by U.S. Food and Drug Administration. The agency notice is the authoritative version — read it before you act, and treat it as the final word if anything here looks different.

Open the FDA — Company recall announcements record U.S. Food and Drug Administration recalls

Questions people ask about this recall

Why was SiluetaYa dietary supplements recalled?

Product contains yellow oleander Ingestion of yellow oleander can cause severe or even fatal neurological, gastrointestinal, and cardiovascular adverse health effects.

How do I know if I have the recalled product?

Match the codes printed on your package against the notice: UPC 7500464462411; lot code US1220; best-by date 06 or 2027. If the code on your package is not on that list, your unit is outside the recall.

What should I do with it right now?

Check the lot number on your pack against the codes listed above.

Can I get my money back?

The notice says: Consumers who purchased tejocote root from the SiluetaYa line are advised not to consume it and to return it to the place of purchase for a full refund.

Which states were affected?

The notice lists Arizona, California, New Mexico, New York, Texas, Utah.

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