Wise Woman Herbals Kava Capsules, 450 mg Kava (Piper met. Root), Dosage: 1 capsule up to 3…
Recalling firm: EarthLab Inc
The microbial test result is found to be out of specification due to high yeast and mold counts.
Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: May 22, 2023.
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748840142848FDA code information
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).
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Full FDA record and distribution details
Original 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.
Extracted codes and context
| Type | Code / value | Context |
|---|---|---|
| UPC | 748840142848 | apsule 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-to |
| lot | 10/22/21 | cates 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). |
Original FDA recall reason
The microbial test result is found to be out of specification due to high yeast and mold counts.
Recall details
- Recall number
- F-1346-2022
- Event ID
- 90203
- FDA status
- Terminated
- Initiated
- May 11, 2022
- Reported
- Jun 29, 2022
- Classified
- Jun 22, 2022
- Terminated
- May 22, 2023
- Quantity
- 1,213 units
- Location
- Creswell, OR, United States
- Initiation type
- Voluntary: Firm initiated
- Notification
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Where it was distributed
nationwide
Data updated September 16, 2026. View official FDA data ↗
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