CLASS I ONGOING Food recall · Reported 1 Apr 2026 · FDA Enforcement Report
Mexican Tejocote Roots Supplement Pieces;; Dietary Supplement recalled
Siluetaya is recalling Mexican Tejocote Roots Supplement Pieces;; Dietary Supplement, distributed in Arizona, California, New Mexico, New York, Texas, Utah. The recall was initiated on 29 Oct 2025 and the FDA has classified it as Class I.
Check your package
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
Recall details
- Recall number
- H-0647-2026
- FDA event ID
- 97947
- Recalling firm
- Siluetaya, Albuquerque, NM
- Brand
- SiluetaYa
- Classification
- Class I
- Status
- Ongoing
- Recall initiated
- 29 Oct 2025
- FDA classified
- 2 Apr 2026
- Reported
- 1 Apr 2026
- Type
- Voluntary: Firm initiated
- Customers notified by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Reason category
- Other Reasons
- Product category
- Dietary Supplements
Timeline
| 29 Oct 2025 | Recall initiated by company | |
| 1 Apr 2026 | Published in enforcement report | +154 days |
| 2 Apr 2026 | Classified by FDA | +1 day |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Product contains yellow oleander
Product as listed by the FDA
SiluetaYa Mexican Tejocote Roots Supplement Pieces; 7g/bottle; Dietary Supplement, UPC#: 7500464462411, Lot: US1220 " Expiration Date: 06/2027
Where it was distributed
Product was distributed directly to consumers via internet sales in AZ, CA, NM, NY, TX, UT
Questions about this recall
Why was it recalled?
Product contains yellow oleander
Which lots are affected?
Lot: US1220, Expiration Date: 06/2027
Where was it sold?
Product was distributed directly to consumers via internet sales in AZ, CA, NM, NY, TX, UT
What should I do if I have it?
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
What does Class I mean?
Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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