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ACTIVE RECALL — CLASS IActive recallH-0647-2026/FDA enforcement
Siluetaya, LLC·Dietary Supplements·Oct 29, 2025

Siluetaya Mexican Tejocote Roots Supplement Pieces

What you need to know

Class I

  • What happened

    Product contains yellow oleander

  • Health risk

    The product has a reasonable probability of causing serious adverse health consequences or death. A safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.

  • Action required

    Stop taking the supplement. Check the lot and UPC codes below, then return it to the retailer or contact the manufacturer about a refund. Seek medical advice if you have concerns about exposure.

Active recall · classified by the FDAIN, AZ, CA, NM +3 moreMore supplements

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Product identification

Source: FDA FOOD

Brand nameSiluetaya, LLC
Recalling firmSiluetaya, LLCAlbuquerque, NM, United States
UPC / barcodes
7 500464 46241 1
Lot / date codes
  • Lot: US1220, Expiration Date: 06/2027
Distribution area
INAZCANMNYTXUT

Product was distributed directly to consumers via internet sales in AZ, CA, NM, NY, TX, UT

United States

Quantity affected40 units
Recall initiationFDA report date: April 1, 2026
FDA recall numberH-0647-2026

Beyond the headline

The recall, in context

Siluetaya, LLC initiated this supplements recall on October 29, 2025. The FDA enforcement report states: Product contains yellow oleander. The FDA report lists distribution as: Product was distributed directly to consumers via internet sales in AZ, CA, NM, NY, TX, UT.

The FDA enforcement report describes the reason as: Product contains yellow oleander

Siluetaya Mexican Tejocote Roots Supplement Pieces was made or distributed by Siluetaya, LLC in Albuquerque, NM, United States. This page reflects FDA report H-0647-2026, dated April 1, 2026.

Why this is a Class I recall

Class I means the product has a reasonable probability of causing serious adverse health consequences or death. In this recall, a safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.

FDA definition

The product has a reasonable probability of causing serious adverse health consequences or death.

What to do now

  1. 1

    Stop using it

    Do not eat, drink or take the affected product.

  2. 2

    Check the codes

    Compare the UPC and lot code against the table above.

  3. 3

    Return or discard

    Contact the retailer or recalling firm about a refund, and dispose of the product safely.

Consumer safety guide

Product safety recall

Symptoms to watch for

The official enforcement report describes the specific risk. Follow the recall notice, check the product codes and do not use a product that may be affected.

Higher-risk groups

Children, pregnant people, older adults and people with weakened immune systems should take extra care when a product's safety is uncertain.

What to do now

  1. 1Stop using or eating the product and keep it away from children and pets.
  2. 2Check the UPC and lot/date codes on this page and follow the official recall notice for disposal or return.
  3. 3Seek medical advice if anyone develops severe or worrying symptoms after exposure.

Read the official source record for the specific hazard and instructions.

This is general consumer safety information, not medical advice or a diagnosis. Follow the official recall notice and contact a healthcare professional if you have concerns about exposure or symptoms.

Frequently asked

Questions about this recall

What is the Siluetaya Mexican Tejocote Roots Supplement Pieces recall?

Siluetaya, LLC recalled Siluetaya Mexican Tejocote Roots Supplement Pieces in an FDA Class I enforcement action reported as H-0647-2026. Product contains yellow oleander

What should I do if I bought this product?

Stop taking the supplement. Check the lot and UPC codes below, then return it to the retailer or contact the manufacturer about a refund. Seek medical advice if you have concerns about exposure. Stop using or eating the product and keep it away from children and pets. Check the UPC and lot/date codes on this page and follow the official recall notice for disposal or return. Seek medical advice if anyone develops severe or worrying symptoms after exposure.

Is the Siluetaya, LLC recall still active?

Yes. As of the latest FDA enforcement report, this recall is listed as ongoing. Check the official source record for the most current status before making a decision.

Where can I verify this recall?

This page is normalized from the openFDA enforcement record H-0647-2026. You can verify it directly using the official source link on this page. VerifyRecall updates its index from public FDA enforcement data and does not replace advice from the FDA, the recalling firm or a healthcare professional.

Verify before you act.

VerifyRecall is independent and not affiliated with the FDA. Always confirm the latest status on the official source record.

Official source

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Record last synced from official openFDA enforcement data on November 14, 2026. Source record: official FDA notice.