Recall Radar · 美国食品召回雷达

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FDA Food Enforcement · Medium / 中

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.

Recall F-1346-2022 · Published 2022-06-29

Official-information notice / 官方信息说明: This page transcribes fields from the named agency record. It is not medical, legal, or food-safety advice. Follow the agency's original notice and instructions.

Recall number / 召回编号

F-1346-2022

Classification / 风险等级

Medium / 中

Published / 发布时间

2022-06-29

Recalling firm / 召回企业

EarthLab Inc

Product description / 产品描述

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.

Product code / 产品代码

Not provided in the official record

Code information / 批次与代码信息

90KACA (90 indicates package size; KA indicates Kava; CA indicates capsule). Lots: 16754, 17157, and 17764-1. Best Used By for each lot: 10/22/21 (for 16754); 10/22/22 (for 17157); 1/26/24 (for 17764-1).

Product quantity / 产品数量

1,213 units

Distribution / 销售地区

nationwide

Reason for recall / 召回原因

The microbial test result is found to be out of specification due to high yeast and mold counts.

Open official source ↗ / 打开官方来源

Last synchronized: 2026-08-09. Recall Radar does not replace agency guidance.