# FDA recall F-1346-2022

> **EarthLab Inc** · Class II · food recall initiated 2022-05-11.

## 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.

## Distribution

nationwide

## Key facts

- **Recall number:** F-1346-2022
- **Recalling firm:** EarthLab Inc
- **Classification:** Class II
- **Product type:** food
- **Status:** Terminated
- **Initiation date:** 2022-05-11
- **Report date:** 2022-06-29
- **Termination date:** 2023-05-22

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Creswell, OR, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=F-1346-2022

## Citation

> AI Analytics. FDA recall F-1346-2022. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/F-1346-2022. Source: US FDA. Licensed CC0.

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*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*
