The Recall Desk
SevereFDA (Food)·F-1165-2024·Announced 2024-04-24

Brazil Seed Dietary Supplement Recalled for Yellow Oleander Contamination

H&NATURAL Brazil Seed supplement containing yellow oleander has been recalled by the FDA as a Class I health hazard. The product was distributed exclusively through internet sales.

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 is classified as FDA Class I, the FDA's highest hazard category for imminent threats to health. Although no illnesses or injuries have been reported, the confirmed presence of yellow oleander—a known toxic substance—in a dietary supplement intended for ingestion warrants the Severe classification.

Plain-English summary

H&NATURAL 2 Pack Brazil Seed supplement (marketed as SEMILLA DE BRASIL) has been recalled by the FDA due to the presence of yellow oleander and its components in the product. The product consists of two yellow boxes, each containing 60 pieces of 5 grams, with expiration dates listed as 05/24 and 03/24. The product does not include a lot code on its label.

Yellow oleander is a toxic substance that poses serious health risks. Its presence in a dietary supplement intended for human consumption creates an imminent health hazard.

The product was distributed exclusively through internet sales. The recalling firm is HandNatural. The full distribution scope remains unknown at this time.

This recall is classified as FDA Class I, indicating the highest category of product hazard.

The recalled product

Product
H&NATURAL 2 PACK! BRAZIL SEED 60 PIECES, PURE NATURAL SEMILLA DE BRASIL FOR 60 DAYS, 5 GRAMS PER BOX, 2 YELLOW BOXES
Manufacturer
HandNatural
Category
Food — Dietary Supplement
Hazard
  • yellow-oleander

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.

Related recalls

Same category