Baby Allergy Herbal Supplement — Class II food recall H-0341-2026
Terminated recall by A New Life Herbs, LLC, reported 2025-12-31, distributed in AL, AZ, CA, GA, IL, IN, MN, MO…. Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label
| Recall number | H-0341-2026 |
|---|---|
| Product type | Food |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | A New Life Herbs, LLC, Somerville, TN, United States |
| Recall initiated | 2025-11-20 |
| Classified | 2025-12-23 |
| Reported by FDA | 2025-12-31 |
| Terminated | 2026-08-28 |
| Distributed | AL, AZ, CA, GA, IL, IN, MN, MO, MS, NC, NY, TN |
| Quantity | 23 bottles |
| Reason classes | labeling, unapproved product |
| UPC / GTIN / UDI-DI | 00249953949282 |
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
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/H-0341-2026. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.