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ACTIVE RECALL — CLASS IActive recallH-1108-2026/FDA enforcement
Shaman Botanicals, LLC·Dietary Supplements·Feb 13, 2026

Product Label Reads in Part as "White Vein Advanced Alkaloids Chewable Tablets 225mg…

What you need to know

Class I

  • What happened

    A sample of the product revealed the active ingredient is in a quantity greater than the labeled specification.

  • 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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Match before you discard

Product identification

Source: FDA FOOD

Brand nameShaman Botanicals, LLC
Recalling firmShaman Botanicals, LLCNorth Kansas City, MO, United States
UPC / barcodes
8 10057 76377 9
Lot / date codes
  • B#AAW.501.3
  • all expiration dates
Distribution area

Firm has provided the following information: 14 wholesalers, 108 Distributors, 46 Company-owned stores, 2202 online customers

United States

Quantity affected97, 063 units
Recall initiationFDA report date: March 25, 2026
FDA recall numberH-1108-2026

Beyond the headline

The recall, in context

Shaman Botanicals, LLC initiated this supplements recall on February 13, 2026. The FDA enforcement report states: A sample of the product revealed the active ingredient is in a quantity greater than the labeled specification. The FDA report lists distribution as: Firm has provided the following information: 14 wholesalers, 108 Distributors, 46 Company-owned stores, 2202 online customers.

The FDA enforcement report describes the reason as: A sample of the product revealed the active ingredient is in a quantity greater than the labeled specification.

Product Label Reads in Part as "White Vein Advanced Alkaloids Chewable Tablets 225mg… was made or distributed by Shaman Botanicals, LLC in North Kansas City, MO, United States. This page reflects FDA report H-1108-2026, dated March 25, 2026.

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 Product Label Reads in Part as "White Vein Advanced Alkaloids Chewable Tablets 225mg… recall?

Shaman Botanicals, LLC recalled Product Label Reads in Part as "White Vein Advanced Alkaloids Chewable Tablets 225mg… in an FDA Class I enforcement action reported as H-1108-2026. A sample of the product revealed the active ingredient is in a quantity greater than the labeled specification.

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 Shaman Botanicals, LLC 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 H-1108-2026. 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

More recalls by Shaman Botanicals, LLC

View brand
Class I·

Shaman Botanicals, LLC

Product Label Reads in Part as "White Vein Advanced Alkaloids Chewable Tablets 15mg…

A sample of the product had the active ingredient in a quantity greater than the labeled specification.

Distribution not listedSupplements

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