RecallRadar

FDA Food recall F-1346-2022

Wise Woman Herbals Kava Capsules, 450 mg Kava (Piper met

On 2022-06-29 the FDA classified a Class II recall of Wise Woman Herbals Kava Capsules, 450 mg Kava (Piper met by Earthlab, citing the microbial test result is found to be out of specification due to high yeast and mold counts.

Read the official FDA Food notice

AgencyFDA Food
Recall numberF-1346-2022
ClassificationClass II
Statusterminated
Initiated2022-05-11
Published2022-06-29
Last updated2026-09-13 11:50 UTC
CompanyEarthlab
DistributionUS

Product

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

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

Identifiers

upc748840142848
code_info
90KACA (90 indicates package size; KA indicates Kava; CA indicates capsule). Lots: 16754, 17157, and 17764-1. Best U…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).

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:50 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1346-2022%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.