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FDA source record Class I Ongoing

ELV Control Herbal Supplement; 90 Capsules

Recall Date: 2024-04-03 Recalling Firm: World Green Nutrition Inc. Record Ref: F-1391-2024

FINDARECALL QUICK READ

What this record tells you

This FDA record concerns ELV Control Herbal Supplement; 90 Capsules and names World Green Nutrition Inc. as the recalling firm. Use the source fields below to narrow the match, then verify the exact item and current remedy on the issuing-agency page.

  • Firm: World Green Nutrition Inc.
  • Classification: Class I
  • Status: Ongoing
  • Recall date: 2024-04-03
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Product Description & Identification

ELV Control Herbal Supplement; 90 Capsules

Reason for Recall / Hazard Identified

FDA Analysis found product labeled as tejocote is actually yellow oleander, which is toxic to humans.

How to Check Whether Your Product Matches

A matching product name or photograph is not enough by itself. Compare every identifier available on your item or packaging with the official notice.

  1. Confirm the full product and brand or recalling-firm name.
  2. Compare package size, color, flavor, model, style, or configuration when listed.
  3. Check UPC, lot, batch, serial, date code, recall number, or USDA establishment number.
  4. Review the recall date and distribution information without assuming every seller is listed.
  5. Open the official FDA source below and follow its current instructions.

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Consumer Action Recorded in the Source

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Distribution & Affected States

Product is sold through authorized dealers and E-commerce throughout the USA and Mexico, While the products, Elv Control Herbal Supplement and Mexican Tejocote Root Supplement Pieces (Raiz de Tejocote Mexicano Suplemento en Trozos), were intended to be distributed only through authorized distributors, it is possible that these products were purchased and further distributed via e-commerce platforms and/ or physical stores.

Verify With the Issuing Agency

This record was last updated in our index on 2026-08-09 21:59:13 UTC. Because recall enforcement statuses and instructions evolve, always verify details directly with the issuing government agency.

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Record Transparency

Issuing agency
FDA
Source ID
F-1391-2024
Indexed update
2026-08-09 21:59:13 UTC
Official source
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