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RECALL RECORD — CLASS IIRecall closedH-0343-2026/FDA enforcement
A New Life Herbs, LLC·Dietary Supplements·Nov 20, 2025

Boswellia Herbal Supplement, 1: 5 Alcohol Double Extract, Extracted from Frankincense With…

What you need to know

Class II

  • What happened

    Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label

  • Health risk

    The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. 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.

Recall closed · classified by the FDAAL, AZ, CA, GA +8 moreMore supplements

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Product identification

Source: FDA FOOD

Brand nameA New Life Herbs, LLC
Recalling firmA New Life Herbs, LLCSomerville, TN, United States
UPC / barcodes
2 84260 39242 0
Lot / date codes
  • T848B EXP 11/30 T836B EXP 10/30 T808B EXP 9/30 T771B EXP 7/30 T723B EXP 3/30 T696B EXP 1/29 T655B EXP 10/29 T594B EXP 4/29 T536B EXP 10/28
Distribution area
ALAZCAGAILINMNMOMSNCNYTN

AL, AZ, CA, GA, IL, IN, MN, MO, MS, NC, NY, TN

United States

Quantity affected278 bottles
Recall initiationFDA report date: December 31, 2025
FDA recall numberH-0343-2026

Beyond the headline

The recall, in context

A New Life Herbs, LLC initiated this supplements recall on November 20, 2025. The FDA enforcement report states: Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label. The FDA report lists distribution as: AL, AZ, CA, GA, IL, IN, MN, MO, MS, NC, NY, TN.

The FDA enforcement report describes the reason as: Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label

Boswellia Herbal Supplement, 1: 5 Alcohol Double Extract, Extracted from Frankincense With… was made or distributed by A New Life Herbs, LLC in Somerville, TN, United States. This page reflects FDA report H-0343-2026, dated December 31, 2025.

Why this is a Class II recall

Class II means the product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. In this recall, a safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.

FDA definition

The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote.

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 Boswellia Herbal Supplement, 1: 5 Alcohol Double Extract, Extracted from Frankincense With… recall?

A New Life Herbs, LLC recalled Boswellia Herbal Supplement, 1: 5 Alcohol Double Extract, Extracted from Frankincense With… in an FDA Class II enforcement action reported as H-0343-2026. Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label

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 A New Life Herbs, LLC recall still active?

The FDA lists this recall as recall closed. It remains relevant if you still have the affected product or need to identify a historical recall.

Where can I verify this recall?

This page is normalized from the openFDA enforcement record H-0343-2026. 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 A New Life Herbs, LLC

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A New Life Herbs, LLC

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