← FDA ENFORCEMENT
H-0341-2026Class II

A New Life Herbs, LLC

What this record is not

A recall record is reproduced as FDA published it, and the classification is FDA’s. SPEQ adds no interpretation, and a recall concerns the products and dates in the record — it is not a statement about a company’s other products or its current status.

Recalling firm
A New Life Herbs, LLC
Product type
Food / supplement / cosmetic
Status
Terminated
Report date
2025-12-31
Distribution
AL, AZ, CA, GA, IL, IN, MN, MO, MS, NC, NY, TN
Firm state
TN
Product quantity
23 bottles
Initiated by
Voluntary: Firm initiated
Reason for recall

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

Product description

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

Code / lot info

E166SA EXP 4/28

Data: U.S. FDA. Recall details are as reported by the FDA. The quality-domain mapping and severity are a SPEQ editorial interpretation of the recall reason, not an official FDA classification. Open the enforcement explorer →