SiluetaYa Mexican Tejocote Roots Supplement Pieces recall (April 2026): reason, lots, what to do
Not medical advice. This page reproduces one FDA enforcement report and explains its fields; FDA’s text is quoted as FDA’s. If you have this product and any symptoms, your pharmacist or doctor comes before this page.
What was recalled
Siluetaya, LLC (Albuquerque, NM) recalled SiluetaYa Mexican Tejocote Roots Supplement Pieces in a recall FDA classified as Class I. FDA’s stated reason: “Product contains yellow oleander”. Started October 29, 2025; posted in the enforcement report April 1, 2026; status Ongoing.
Class I means, in FDA’s words, a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death. Distribution: “Product was distributed directly to consumers via internet sales in AZ, CA, NM, NY, TX, UT”. Quantity: 40 units. Check your lot →
The FDA record
Everything in this table is copied from FDA’s enforcement report for event 97947, retrieved from openFDA on September 21, 2026; the last row links to the live record so you can confirm it has not changed.
| Recalling firm | Siluetaya, LLC, Albuquerque, NM |
|---|---|
| Product | SiluetaYa Mexican Tejocote Roots Supplement Pieces; 7g/bottle; Dietary Supplement, UPC#: 7500464462411, Lot: US1220 " Expiration Date: 06/2027 |
| Reason for recall (FDA’s text) | “Product contains yellow oleander” |
| Classification | Class I |
| Status | Ongoing |
| Recall type | Voluntary: Firm initiated |
| Recall initiated | 2025-10-29 |
| Enforcement report date | 2026-04-01 |
| FDA classified on | 2026-04-02 |
| Distribution | Product was distributed directly to consumers via internet sales in AZ, CA, NM, NY, TX, UT |
| Quantity | 40 units |
| How the firm notified | Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit |
| Recall number | H-0647-2026 |
Lots, codes and how to check your bottle
FDA’s “code info” field for this event, verbatim:
Lot: US1220, Expiration Date: 06/2027
Find the lot number on the bottom of the container, beside the seal or on the box flap; the expiration date is usually printed next to it. If the code on your container appears above, it is in scope. If the product name matches but the code does not, your unit is not part of this recall, though a second lot is sometimes added later, so re-check the recall list before finishing the bottle.
Why this is a Class I recall
FDA assigns the class by the probability and severity of harm, not by how much product is involved. For this event the reason falls into what we file as hidden drug or prohibited ingredient: a substance that is not a lawful dietary ingredient was found in, or substituted for, the product. This is the recall category with the least warning for the buyer: the label reads like a supplement and the effect comes from something else.
FDA’s definition of Class I (21 CFR 7.3) is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death. A Class I recall is the strongest signal FDA sends about a consumer product short of a seizure; it is reserved for the cases where continuing to use the product is itself the risk. The reason text is the authority for this specific event; the class is FDA’s summary judgement of it.
If you bought it
- Stop taking it now; for a Class I recall this is the point of the notice.
- Match your lot against the codes above. Keep the container: the firm’s notice normally offers a refund on proof of the lot number or a photo.
- If you take prescription medicines, tell your pharmacist which product you were taking; an undeclared ingredient can interact with what you are prescribed. Then report to FDA MedWatch (online form or 1-800-FDA-1088).
- Check the firm’s other products. A recall event often expands to the same firm’s other SKUs a week or two later. Search “Siluetaya, LLC” on the full recall list.
Choosing a replacement that can be checked
This product does not name an ingredient we track, so there is no like-for-like guide to send you to. The general rule holds: the only supplements whose contents a buyer can verify are those in a certifier’s public registry (NSF/ANSI 173, NSF Certified for Sport, USP Verified, Informed Sport) or with a lot-specific certificate of analysis the brand publishes. Our registry audit shows how few products clear that bar, and the per-ingredient third-party-tested pages (magnesium, creatine, vitamin D, omega-3, multivitamins) list the ones that do.
Frequently asked questions
Why was SiluetaYa Mexican Tejocote Roots Supplement Pieces recalled?
FDA's enforcement report gives the reason as: "Product contains yellow oleander". FDA records the recall type as "Voluntary: Firm initiated"; Siluetaya, LLC of Albuquerque, NM started it October 29, 2025 and it was posted in FDA's enforcement report on April 1, 2026 as Class I.
Which lots of SiluetaYa Mexican Tejocote Roots Supplement Pieces are affected?
FDA's record lists: Lot: US1220, Expiration Date: 06/2027. Match these against the lot number, UPC or expiration date printed on your container; a bottle whose code is not listed is not part of this recall.
Where was SiluetaYa Mexican Tejocote Roots Supplement Pieces sold?
FDA's record gives the distribution as: "Product was distributed directly to consumers via internet sales in AZ, CA, NM, NY, TX, UT". Quantity recalled: 40 units.
Is this recall over?
FDA lists the status as "Ongoing". Ongoing means the firm is still retrieving product from the market.
← Every FDA dietary supplement recall since 2023 · How we score supplement safety
Sources
- U.S. Food and Drug Administration. Enforcement report, event 97947, recall number H-0647-2026. Via openFDA Food Enforcement API, retrieved September 21, 2026. H-0647-2026
- 21 CFR 7.3(m): recall classification definitions. eCFR Title 21 Part 7.
- FDA. MedWatch: The FDA Safety Information and Adverse Event Reporting Program. fda.gov/safety/medwatch.