What happened
Original notice title
SiluetaYa Recalls Tejocote Product Because of Possible Health Risk
From the archived source record
When a company announces a recall, market withdrawal, or safety alert, the FDA posts the company's announcement as a public service. FDA does not endorse either the product or the company. More Recalls, Market Withdrawals, & Safety Alerts Recalls, Market Withdrawals, & Safety Alerts Recall Resources Enforcement Reports Industry Guidance For Recalls Major Product Recalls SiluetaYa is recalling its tejocote root because FDA analysis has determined that the products appear to be Thevetia peruviana, or yellow oleander. All parts of the yellow oleander plant are known to contain cardiac glycosides, which are highly toxic to humans and animals. Ingestion of yellow oleander can cause severe or even fatal neurological, gastrointestinal, and cardiovascular adverse health effects. Symptoms may include nausea, vomiting, dizziness, diarrhea, abdominal pain, changes in heart rhythm, arrhythmia, and more. The recall was the result of sampling conducted by the FDA. Regulated Product(s) Dietary Supplements Follow FDA Follow @US_FDA on X Follow FDA on Facebook Follow @FDArecalls on X Recent Recalled Product Photos on FDA's Flickr Photostream Recent Recalled Product Photos on FDA's Flickr Photostream
What the official notice says to do
Check the original notice for the instructions that apply to the named product, company, and affected lots.
Read the official notice →Status and source details
- Status recorded in the archive
- Published recall notice
- Source checked
- Jul 16, 2026
- Record revision
- df0d620f1a42
This is a dated record. Its current status may have changed since the source was captured. A record applies to its stated scope; it is not a safety rating for every product from a company.
Sources, dates, and coverage →