ACTIVE RECALL — CLASS IActive recallF-1391-2024/FDA enforcement

Elv Control Herbal Supplement

What you need to know

Class I
  • What happened

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

  • Health risk

    The product has a reasonable probability of causing serious adverse health consequences or death. A safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.

  • Action required

    Stop taking the supplement. Check the lot and UPC codes below, then return it to the retailer or contact the manufacturer about a refund. Seek medical advice if you have concerns about exposure.

Active recall · classified by the FDADE, ORMore supplements

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Product identification

Source: FDA FOOD

Brand nameWorld Green Nutrition INC.
Recalling firmWorld Green Nutrition INC.San Antonio, TX, United States
UPC / barcodes
1 082701 05032 82 40622 07132 40 50722 07132 41 90620 23000 9
Lot / date codes
  • N1082701 050328; GESPM240622 071324; GESPM300; 622 071324; GESPM050722 071324; 190620230009B 061928
  • 190620231573678B 062828280620231; 573678BA 062828
Distribution area
DEOR

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.

United States, Mexico

Quantity affected20, 092 units
Recall initiationFDA report date: July 3, 2024
FDA recall numberF-1391-2024

Beyond the headline

The recall, in context

World Green Nutrition INC. initiated this supplements recall on April 3, 2024. The FDA enforcement report states: FDA Analysis found product labeled as tejocote is actually yellow oleander, which is toxic to humans. The FDA report lists distribution as: 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.

The FDA enforcement report describes the reason as: FDA Analysis found product labeled as tejocote is actually yellow oleander, which is toxic to humans.

Elv Control Herbal Supplement was made or distributed by World Green Nutrition INC. in San Antonio, TX, United States. This page reflects FDA report F-1391-2024, dated July 3, 2024.

Why this is a Class I recall

Class I means the product has a reasonable probability of causing serious adverse health consequences or death. In this recall, a safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.

FDA definition

The product has a reasonable probability of causing serious adverse health consequences or death.

What to do now

  1. 1

    Stop using it

    Do not eat, drink or take the affected product.

  2. 2

    Check the codes

    Compare the UPC and lot code against the table above.

  3. 3

    Return or discard

    Contact the retailer or recalling firm about a refund, and dispose of the product safely.

Consumer safety guide

Product safety recall

Symptoms to watch for

The official enforcement report describes the specific risk. Follow the recall notice, check the product codes and do not use a product that may be affected.

Higher-risk groups

Children, pregnant people, older adults and people with weakened immune systems should take extra care when a product's safety is uncertain.

What to do now

  1. 1Stop using or eating the product and keep it away from children and pets.
  2. 2Check the UPC and lot/date codes on this page and follow the official recall notice for disposal or return.
  3. 3Seek medical advice if anyone develops severe or worrying symptoms after exposure.

Read the official source record for the specific hazard and instructions.

This is general consumer safety information, not medical advice or a diagnosis. Follow the official recall notice and contact a healthcare professional if you have concerns about exposure or symptoms.

Frequently asked

Questions about this recall

What is the Elv Control Herbal Supplement recall?

World Green Nutrition INC. recalled Elv Control Herbal Supplement in an FDA Class I enforcement action reported as F-1391-2024. FDA Analysis found product labeled as tejocote is actually yellow oleander, which is toxic to humans.

What are the symptoms of Product safety recall exposure?

The official enforcement report describes the specific risk. Follow the recall notice, check the product codes and do not use a product that may be affected.

Who is most at risk from Product safety recall?

Children, pregnant people, older adults and people with weakened immune systems should take extra care when a product's safety is uncertain.

What should I do if I bought this product?

Stop taking the supplement. Check the lot and UPC codes below, then return it to the retailer or contact the manufacturer about a refund. Seek medical advice if you have concerns about exposure. Stop using or eating the product and keep it away from children and pets. Check the UPC and lot/date codes on this page and follow the official recall notice for disposal or return. Seek medical advice if anyone develops severe or worrying symptoms after exposure.

How do I get a refund from World Green Nutrition INC.?

Contact the recalling company or the retailer where you purchased the product, quote the FDA recall number and ask about a refund or replacement. Keep the packaging, lot code and proof of purchase where possible. The FDA does not issue consumer refunds. Reference FDA recall F-1391-2024 and keep the packaging, lot code and proof of purchase if you have them.

Is the World Green Nutrition INC. recall still active?

Yes. As of the latest FDA enforcement report, this recall is listed as ongoing. Check the official source record for the most current status before making a decision.

Where can I verify this recall?

This page is normalized from the openFDA enforcement record F-1391-2024. You can verify it directly using the official source link on this page. VerifyRecall updates its index from public FDA enforcement data and does not replace advice from the FDA, the recalling firm or a healthcare professional.

Verify before you act.

VerifyRecall is independent and not affiliated with the FDA. Always confirm the latest status on the official source record.

Official source

Brand history

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Record last synced from official openFDA enforcement data on November 14, 2026. Source record: official FDA notice.