The Recall Desk
SevereFDA (Food)·F-1161-2024·Announced 2024-04-24

H&Natural Tejocote Root Supplement Recalled for Yellow Oleander Contamination

H&Natural is recalling its tejocote root supplement because the product contains yellow oleander and its components. Consumers should not use this supplement.

What this means for you

Illness, injury, or structural failure has been reported. Stop using the product immediately and contact the manufacturer for a refund or repair.

Our severity reasoning: This recall received an FDA Class I classification, which the recall rules specify establishes a minimum severity score of 4. No illnesses, injuries, or deaths have been reported in the source text, which prevents assignment of the Critical (5) score.

Plain-English summary

H&Natural is recalling its Tejocote Root supplement (marketed as a 90-piece, 3-month supply) because the product contains yellow oleander and its components.

Yellow oleander is a toxic plant, and its presence in the supplement poses a significant health risk. The FDA has classified this as a Class I recall, indicating the most serious level of hazard.

The product was distributed exclusively through internet sales. The full scope and scale of distribution remain unknown.

Consumers who purchased this product should not use it. Those with the product are advised to discard it or contact the seller for return or refund instructions.

The recalled product

Product
H&NATURAL TEJOCOTE ROOT 90 PIECES, 3 MONTH SUPPLY, PURE AND NATURAL RAIZ DE TEJOCOTE SUPPLEMENT FOR WOMEN AND MEN.
Manufacturer
HandNatural
Category
Food — Dietary Supplement
Hazard
  • yellow-oleander
  • poison

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.

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