Food Recall Check
Class II · Moderate risk Terminated Initiated Nov 20, 2025 (11 months ago)

Boswellia Herbal Supplement recall

Recalled by A New Life Herbs, LLC · Somerville, TN, United States

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

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

A label that does not match the product can hide an ingredient someone must avoid, or show a wrong use-by date. All labeling errors recalls.

What was recalled

Boswellia Herbal Supplement, 1:5 Alcohol Double Extract, Extracted from Frankincense with powerful anti-inflammatory properties, useful for pain & inflammation; packaged in a 2 oz. glass dropper bottle, UPC 284260392420

Quantity: 278 bottles

Food: Dietary supplements

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

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

Where it was sold

Alabama Arizona California Georgia Illinois Indiana Minnesota Missouri Mississippi North Carolina New York Tennessee

FDA's distribution note: AL, AZ, CA, GA, IL, IN, MN, MO, MS, NC, NY, TN

Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm
A New Life Herbs, LLC
Initiated by
Voluntary: Firm initiated
Recall initiated
Nov 20, 2025
In FDA report of
Dec 31, 2025
Terminated
Aug 28, 2026
FDA recall number
H-0343-2026 · event 98037
Official record
FDA enforcement report search

Also recalled with it (8 more products)

FDA files each product of one recall action separately; these share the same FDA event.

Class II · Moderate risk Terminated Labeling

Anti-virus Herbal Supplement

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

A New Life Herbs, LLC 12 states H-0340-2026
Class II · Moderate risk Terminated Labeling

Baby Allergy Herbal Supplement

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

A New Life Herbs, LLC 12 states H-0341-2026
Class II · Moderate risk Terminated Labeling

Baby Soothe Herbal Supplement

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

A New Life Herbs, LLC 12 states H-0342-2026
Class II · Moderate risk Terminated Labeling

Chaga Mushroom Herbal Supplement

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

A New Life Herbs, LLC 12 states H-0344-2026
Class II · Moderate risk Terminated Labeling

Ear Drops Herbal Supplement

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

A New Life Herbs, LLC 12 states H-0345-2026
Class II · Moderate risk Terminated Labeling

Organic Ginger Root Herbal Supplement

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

A New Life Herbs, LLC 12 states H-0346-2026
Class II · Moderate risk Terminated Labeling

Pain Away Herbal Supplement

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

A New Life Herbs, LLC 12 states H-0347-2026
Class II · Moderate risk Terminated Labeling

Sinus Cap Herbal Supplement

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

A New Life Herbs, LLC 12 states H-0348-2026