HandNatural is recalling several varieties of H&NATURAL Tejocote Root and Brazil Seed dietary supplements because testing discovered the presence of yellow oleander, a poisonous plant. These products were sold exclusively online in various package sizes including 30-piece bottles and boxes, 90-piece boxes, and 180-piece two-packs. Affected items have expiration dates of March 2024 or May 2024, though no lot codes are printed on the labels.
The products contain yellow oleander, a toxic plant that can cause severe illness or death. Consumption can lead to nausea, vomiting, dizziness, diarrhea, abdominal pain, and dangerous heart rhythm changes.
You have 2 options:
Recall #: F-1158-2024
Recall #: F-1159-2024
Recall #: F-1160-2024. Pure and natural Raiz de Tejocote supplement.
Recall #: F-1161-2024. 3 month supply.
Recall #: F-1162-2024. 5 grams per box.
Recall #: F-1163-2024. 5 grams per bottle.
Recall #: F-1164-2024. 5 grams per box.
Recall #: F-1165-2024
Recall #: F-1166-2024
Recall #: F-1167-2024
Recall #: F-1168-2024
Recall #: F-1169-2024
Recall #: F-1170-2024
Recall #: F-1171-2024
Recall #: F-1172-2024
Image 1 - Labeling, Brazil Seed H& Natural 30 day supply, yellow label
Image 2 - Labeling, Brazil Seed, Facts Panel, yellow label
Image 3 - Labeling, Brazil Seed, Facts Panel, black label
Image 4 - Labeling, Brazil Seed, H& Natural, 30 day supply, black label
Image 5 - Labeling, Brazil Seed, H& Natural 30 day supply paper board packet, green
Image 6 - Labeling, Brazil Seed, H&Natural 30 day supply paper board packet orange
Image 7 - Labeling, Brazil Seed suggested Use
Image 8 - Labeling, Tejo Root, nutrition facts panel
Image 9 - Labeling, Tejo Root Front
If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.
This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.
AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.
Sources: FDA iRES · FDA Press Release · Raw API Response
openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.