Wise Woman Herbals Standardized Kava Glycerite, product is liquid and contains 15 mg…
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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748840142794FDA code information
2PIGL, 4PIGL, 8PIGL, 16PIGL, 32PIGL. (1st digit indicates package size; PI indicates Piper, Latin name of Kava; GL indicates Glycerite). Lots: 17816, 17391, 16988, 16872, 16742. Best Used By for each lot: 9/10/23 (for 17816); 10/2/22 (for 17391); 10/24/21 (for 16988); 8/7/21 (for 16872); 4/25/21 (for 16742).
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Full FDA record and distribution details
Original product description
Wise Woman Herbals Standardized Kava Glycerite, product is liquid and contains 15 mg Kavalactones (from Piper methysticum) and 9 mg Kavalactones (from Piper methysticum) depending on lot. Dosage: 60 drops 1-2 times a day. Product is packaged in Amber Glass Boston Round bottle, Black serrated polypropylene dropper assembly with rubber bulb (2oz only) or Black serrated phenolic lid with polypropylene cone insert (4oz and larger), Clear neck band, Wise Woman Herbals label. Each size has the following UPCs: 2 oz UPC 7 48840 14275 6 4 oz UPC 7 48840 14276 3 8 oz UPC 7 48840 14277 0 16 oz UPC 7 48840 14278 7 32 oz UPC 7 48840 14279 4
Extracted codes and context
| Type | Code / value | Context |
|---|---|---|
| UPC | 748840142794 | 7 48840 14276 3 8 oz UPC 7 48840 14277 0 16 oz UPC 7 48840 14278 7 32 oz UPC 7 48840 14279 4 |
| lot | 9/10/23 | cerite). Lots: 17816, 17391, 16988, 16872, 16742. Best Used By for each lot: 9/10/23 (for 17816); 10/2/22 (for 17391); 10/24/21 (for 16988); 8/7/21 (for 16872); 4/25/21 (for 16742). |
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-1347-2022
- Event ID
- 90203
- FDA status
- Terminated
- Initiated
- May 11, 2022
- Reported
- Jun 29, 2022
- Classified
- Jun 22, 2022
- Terminated
- May 22, 2023
- Quantity
- 2 fl oz = 704 units; 4 fl oz = 262 units; 8 fl oz = 65 units; 16 fl oz = 30 units; 32 fl oz = 1 unit
- 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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