Recall of SiluetaYa Mexican Tejocote Roots Supplement Due to Toxic Substance
Areazine synthesizes this FDA recall directly from FDA's official public data feed. See our methodology for full source attribution and refresh cadence.
Siluetaya, LLC is recalling its SiluetaYa Mexican Tejocote Roots Supplement because it contains yellow oleander, posing a serious health risk. The recall affects 40 units distributed in several U.S. states.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on April 7, 2026 and geographically references United States (AZ, CA, NM, NY, TX, UT). Its severity classification of "high" signals how the issuing agency weighs the risk of harm if no action is taken - "critical" and "high" tier alerts typically carry direct consumer actions, while "medium" and "low" tend toward informational guidance or monitoring advisories. The category it belongs to - FDA Recalls - determines the consumer-protection framework behind it, which shapes what remedies (refunds, replacements, repairs, or the recall itself) are available to affected consumers and which agency holds statutory responsibility for enforcement.
Most readers skim a notice like this, check whether they are personally affected, and move on. The more useful lens is to verify its scope, source, and timestamp, then compare related notices without assuming that one record proves a broader trend.
Areazine pairs this record with the original agency URL so you can check the primary source before acting. Its related labels are recall, product-safety, fda, Food.
Recall of SiluetaYa Mexican Tejocote Roots Supplement
What Happened
Siluetaya, LLC is recalling its SiluetaYa Mexican Tejocote Roots Supplement Pieces because the product contains yellow oleander, a toxic substance.
Which Products Are Affected
The affected product is SiluetaYa Mexican Tejocote Roots Supplement Pieces, 7g per bottle, a dietary supplement with UPC: 7500464462411, Lot: US1220, and Expiration Date: 06/2027. Approximately 40 units were distributed directly to consumers via internet sales in Arizona, California, New Mexico, New York, Texas, and Utah. The official recall number is H-0647-2026.
What You Should Do
Consumers who have purchased the affected product should immediately stop using it and contact Siluetaya, LLC for instructions on returns or refunds. The company is located at 320 Gold Ave SW Ste 620, Albuquerque, NM 87102-3210.
Why This Matters
This recall is classified as Class I by the FDA, indicating a high risk of serious adverse health consequences due to the presence of yellow oleander in the supplement.
Source
Information from the FDA recall notice. Attribution: FDA (Recall Number: H-0647-2026)
Original source: FDA Official Notice ↗
Related FDA Recalls
All FDA Recalls →Nationwide notices with similar length or severity timing 8
Two Areazine-derived peer sets for this FDA recall: nearest notices by body length and by same severity near the same agency date. Peers come from other categories so they are not the same-feed Related list above.
Similar body length
Nearest notices by article body length (1,159 characters here).
Similar severity timing
Same severity (high) notices issued closest in time to April 7, 2026.
Frequently Asked Questions
Common questions about this FDA recall.