Wise Woman Herbals Kava Capsules recalled over mold contamination
- Recall date
- May 11, 2022
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Official notice title
- EarthLab Inc recalls Wise Woman Herbals Kava Capsules, 450 mg Kava (Piper met. Root), Dosage: 1 capsule up to 3 times per day day at 450mg K…
- Recall number
- F-1346-2022
- FDA classification
- Class II
- Brand / firm
- EarthLab Inc
- Sold / distributed
- nationwide
Why it was recalled
The microbial test result is found to be out of specification due to high yeast and mold counts.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
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.
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