Tejocote Root Dietary Supplement Recalled Due to Yellow Oleander
H&Natural is recalling tejocote root supplement due to the presence of yellow oleander and its components. The product was distributed exclusively through internet sales.
What this means for you
Highest-severity recall. Risk of serious injury or death is documented or strongly suspected. Stop using the product now and follow the agency's instructions.
Our severity reasoning: This is an FDA Class I recall, which by agency classification indicates a serious health hazard due to the presence of yellow oleander and its components in the product.
Plain-English summary
H&Natural is recalling the H&NATURAL TEJOCOTE ROOT TWO PACK 180 PIECES supplement. This is a 6-month supply product marketed for women and men. Products carrying expiration dates of 05/24 and 03/24 are included in the recall.
The recall is due to the presence of yellow oleander and its components in the product. The FDA has classified this as a Class I recall, indicating a serious health hazard.
The product was distributed exclusively through internet sales. Consumers who have obtained this product should stop using it immediately and dispose of it safely. Those who have already consumed the product should contact a healthcare provider.
The recalled product
- Product
- H&NATURAL TEJOCOTE ROOT TWO PACK 180 PIECES, 6 MONTH SUPPLY, PURE AND NATURAL RAIZ DE TEJOCOTE SUPPLEMENT FOR WOMEN AND MEN.
- Manufacturer
- HandNatural
- Category
- Food — Dietary Supplement
- Hazard
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- No Lot code on label. Expiration date listed as 05/24 and 03/24.
Distribution
Distribution scope not specified by the agency.
Part of a larger recall action
This product is one of 15 recalled by HandNatural under a single FDA (Food) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
See all 15 products in this recall →Related recalls
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