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ACTIVE RECALL — CLASS IActive recallF-1158-2024/FDA enforcement
Handnatural·Dietary Supplements·Feb 9, 2024

H&natural Tejocote Root Dietary Supplement NET WT 0.36 OZ (10g)

What you need to know

Class I

  • What happened

    Product is being recalled due to the presence of yellow oleander and its components in the product.

  • 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 FDADistribution not listedMore supplements

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Product identification

Source: FDA FOOD

Brand nameHandnatural
Recalling firmHandnaturalSan Luis, AZ, United States
UPC / barcodesNo UPC listed in the FDA enforcement record.
Lot / date codes
  • No Lot code on label. Expiration date listed as 05/24 & 03/24
Distribution area

Firm is 100% internet sales. Distribution is unknown at this time.

United States

Quantity affectedUnknown at this time
Recall initiationFDA report date: April 24, 2024
FDA recall numberF-1158-2024

Beyond the headline

The recall, in context

Handnatural initiated this supplements recall on February 9, 2024. The FDA enforcement report states: Product is being recalled due to the presence of yellow oleander and its components in the product. The FDA report lists distribution as: Firm is 100% internet sales. Distribution is unknown at this time.

The FDA enforcement report describes the reason as: Product is being recalled due to the presence of yellow oleander and its components in the product.

H&natural Tejocote Root Dietary Supplement NET WT 0.36 OZ (10g) was made or distributed by Handnatural in San Luis, AZ, United States. This page reflects FDA report F-1158-2024, dated April 24, 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 lot and date codes 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 H&natural Tejocote Root Dietary Supplement NET WT 0.36 OZ (10g) recall?

Handnatural recalled H&natural Tejocote Root Dietary Supplement NET WT 0.36 OZ (10g) in an FDA Class I enforcement action reported as F-1158-2024. Product is being recalled due to the presence of yellow oleander and its components in the product.

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.

Is the Handnatural 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-1158-2024. 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.