Wise Woman Herbals Kava Capsules — Class II food recall F-1346-2022
Terminated recall by EarthLab Inc, reported 2022-06-29, distributed nationwide. The microbial test result is found to be out of specification due to high yeast and mold counts.
| Recall number | F-1346-2022 |
|---|---|
| Product type | Food |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | EarthLab Inc, Creswell, OR, United States |
| Recall initiated | 2022-05-11 |
| Classified | 2022-06-22 |
| Reported by FDA | 2022-06-29 |
| Terminated | 2023-05-22 |
| Distributed | Nationwide (US) |
| Quantity | 1,213 units |
| Reason classes | microbial contamination, specification failure |
| Pathogens | mold, yeast |
| UPC / GTIN / UDI-DI | 00748840142848 |
| Lot numbers | 16754, 17157, 17764-1 |
Product
Wise Woman Herbals Kava Capsules, 450 mg Kava (Piper met. Root), Dosage: 1 capsule up to 3 times per day day at 450mg Kava root. 90 counts per bottle. UPC 7 48840 14284 8. Kava Capsules older lots are packaged in 250cc Wide Mouth Amber Glass Packer, Black 45/400 PP ribbed skirt screw-top lid, clear neck band, Wise Woman Herbals Large botanical label. Kava Capsules newer lots are packaged in White polypropylene packer style bottle, White serrated flat-topped lid with foam liner, clear neckband, Wise Woman Herbals label.
Reason for recall
The microbial test result is found to be out of specification due to high yeast and mold counts.
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/F-1346-2022. 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.