Boswellia Herbal Supplement — Class II food recall H-0343-2026
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-0343-2026 |
|---|---|
| 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 | 278 bottles |
| Reason classes | labeling, unapproved product |
| UPC / GTIN / UDI-DI | 00284260392420 |
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
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-0343-2026. 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.