SiluetaYa Mexican Tejocote Roots Supplement Pieces; 7g/bottle; Dietary Supplement, UPC#: 7500464462411, Lot: US1220 " E
Summary
The FDA issued a Class I for SiluetaYa Mexican Tejocote Roots Supplement Pieces; 7g/bottle; Dietary Supplemen by Siluetaya, LLC. Reason: Product contains yellow oleander.
Details
Source
Food Recall
External ID
H-0647-2026
Action Date
2026-04-01
Status
Ongoing
Category
food
Product Description
SiluetaYa Mexican Tejocote Roots Supplement Pieces; 7g/bottle; Dietary Supplement, UPC#: 7500464462411, Lot: US1220 " Expiration Date: 06/2027
Lot/Code Info: Lot: US1220, Expiration Date: 06/2027
Quantity Affected: 40 units
Reason for Recall
Product contains yellow oleander
Distribution
Product was distributed directly to consumers via internet sales in AZ, CA, NM, NY, TX, UT
Type: Voluntary: Firm initiated
Recall Initiated: 2025-10-29
Company
Albuquerque, NM
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 64 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Siluetaya, LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Siluetaya, LLC have FDA actions?
This is the only FDA action we have on record for Siluetaya, LLC in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0647-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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