SiluetaYa Mexican Tejocote Roots Supplement Pieces; 7g/bottle; Dietary Supplement, UPC#…

Siluetaya, LLC recalled this product and the FDA reported the enforcement action on 1 April 2026 as Class I. The recall was initiated by the firm. Product contains yellow oleander

The record

Every field below is published by the FDA in the openFDA food enforcement database. Check the FDA notice before acting on any recall: this page is a reading of the public record, not a substitute for it.

Product

SiluetaYa Mexican Tejocote Roots Supplement Pieces; 7g/bottle; Dietary Supplement, UPC#: 7500464462411, Lot: US1220 " Expiration Date: 06/2027

UPC

7500464462411

Reason for recall

Product contains yellow oleander

Recalling firm

Siluetaya, LLC

Firm location

Albuquerque, New Mexico, United States

Classification

Class I

Status

Ongoing

Recall number

H-0647-2026

Quantity

40 units

Distribution

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

Initiated

29 October 2025

Reported by FDA

1 April 2026

Firm notified by

Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Product codes

Lot: US1220, Expiration Date: 06/2027

Reading this record

Five things about this record are not in the record itself, and each one changes how it should be read.

• Class I means the FDA judged a reasonable probability that the product would cause serious health consequences or death. The class is assigned by an agency health hazard evaluation under 21 CFR 7.41, not by the firm.
• The firm started this recall itself. Most FDA food recalls are voluntary, and a recall is a food safety plan working rather than failing. The circumstances in which the agency asks for one instead are set out in 21 CFR 7.45.
• This record is the only one the FDA opened for its recall event, so it covers a single product code.
• This recall has no termination date on the record, so as published it had not been terminated under 21 CFR 7.55.
• The distribution pattern names 5 states, and the FDA published the enforcement report 5 months after the firm began the recall.
• Dietary supplements are regulated under their own good manufacturing practice rule, 21 CFR part 111, and they are the only food category where the dominant recall reason is an ingredient that was never declared because it is a pharmaceutical.

Named in the distribution pattern: California, New Mexico, New York, Texas, Utah. Those pages count recalls by where the RECALLING FIRM sits, which is a different question from where this product went.

Filed under dietary supplements. A product can sit in more than one.

Other dietary supplements recalls

These are the closest records in the corpus: the same kind of food. Unlike the firm’s own records below, they come from different companies, which is what makes them a pattern rather than a history.

All 2026 recalls · All FDA food recall data