FDA recall H-0341-2026 · Dec 31, 2025
A New Life Herbs, LLC: Baby Allergy Herbal Supplement recall
Product
Baby Allergy Herbal Supplement, Contains: Echinacea Purpurea, Oregon Grape Root, Dandelion & Burdock Root, Fenugreek, Ginger Root in vegetable glycerin; packaged in a 2 oz. glass dropper bottle, UPC 249953949282
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
- E166SA EXP 4/28
- Quantity
- 23 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-0341-2026 · search recall number H-0341-2026 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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