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Class II: temporary or reversible health riskTerminated

EarthLab Wise Woman Herbals Kava Capsules Recall

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

EarthLab Inc · Creswell, OR

Risk level
Class II
Reported by FDA
Jun 29, 2022
Recall ID
F-1346-2022
Check your lot numberHow we source this data

Summary

EarthLab recalled Wise Woman Herbals Kava Capsules starting May 11, 2022. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report F-1346-2022 on Jun 29, 2022. Reason: The microbial test result is found to be out of specification due to high yeast and mold counts. Status: Terminated.

Why it was recalled

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

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.

Lot numbers, UPCs & expiration codes

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).

Where it was sold

nationwide

What to do if you have this product

  • Compare the brand, size, and lot/UPC codes on your package with the codes above.
  • If it matches, don't eat it. Return it to the store for a refund or throw it away.
  • Wash surfaces and containers that touched the product.
  • If you feel sick after eating it, contact your doctor. In an emergency call 911.

Recall details

Recall number
F-1346-2022
Classification
Class II
Status
Terminated
Recall initiated
May 11, 2022
FDA report date
Jun 29, 2022
Quantity
1,213 units
Recall type
Voluntary: Firm initiated
Recalling firm
EarthLab Inc

Original FDA data

Every field from FDA enforcement report F-1346-2022, exactly as published.

Show all FDA fields
City
Creswell
State
OR
Status
Terminated
Country
United States
Event ID
90203
Address
185 N Mill St
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).
Postal code
97426-9888
Report date
Jun 29, 2022
Product type
Food
Recall number
F-1346-2022
Classification
Class II
Recalling firm
EarthLab Inc
Product quantity
1,213 units
Termination date
May 22, 2023
Reason for recall
The microbial test result is found to be out of specification due to high yeast and mold counts.
Voluntary / mandated
Voluntary: Firm initiated
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.
Distribution pattern
nationwide
Recall initiation date
May 11, 2022
Initial firm notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Center classification date
Jun 22, 2022

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-1346-2022, published Jun 29, 2022. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

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