PlainRecalls
FDA Food Moderate Class II Terminated

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 neck

Reported: June 29, 2022 Initiated: May 11, 2022 #F-1346-2022

Product Description

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.

Details

Recalling Firm
EarthLab Inc
Units Affected
1,213 units
Distribution
nationwide
Location
Creswell, OR

Frequently Asked Questions

What product 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.. Recalled by EarthLab Inc. Units affected: 1,213 units.
Why was this product recalled? ▼
The microbial test result is found to be out of specification due to high yeast and mold counts.
Which agency issued this recall? ▼
This recall was issued by the FDA Food on June 29, 2022. Severity: Moderate. Recall number: F-1346-2022.

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