FDA recall H-0343-2026 · Dec 31, 2025
A New Life Herbs, LLC: Boswellia Herbal Supplement recall
Product
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
Reason for recall
Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label
What to do
FDA enforcement reports don't include consumer instructions. Check the codes below against your package, and look for the company's notice on FDA's recalls page. If you have the product and aren't sure, don't use it until you've checked.
Recall details
- FDA classification
- Class II: use of or exposure to the product may cause temporary or medically reversible health problems, or the chance of serious problems is remote.
- Status
- Terminated
- Codes, lots and dates
- 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
- Quantity
- 278 bottles
- Distribution
- AL, AZ, CA, GA, IL, IN, MN, MO, MS, NC, NY, TN
- Recalling firm
- A New Life Herbs, LLC, Somerville, TN
- Voluntary or mandated
- Voluntary: Firm initiated
- Recall started
- 2025-11-20
Source: openFDA enforcement record H-0343-2026 · search recall number H-0343-2026 in FDA's Enforcement Report.
Copied from the agency record without changes. Data as of Oct 14, 2026, 1:15 AM EDT. The agency notice is the final word.
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