Food recall

Yerba Prima Inc recall: Great Plains Bentonite + Herbal Detox Capsules 60 capsules

Yerba Prima Inc, of Ashland, OR, recalled Great Plains Bentonite + Herbal Detox Capsules 60 capsules. The FDA's reason: “Potential contamination with Pseudomonas aeruginosa.” The FDA classified it Class II: it could cause temporary or minor harm. The company began the recall voluntarily on June 10, 2025, and the FDA first listed it in its Enforcement Report of June 25, 2025. The FDA has closed the recall: it found the company did all it reasonably could to remove or correct the product.

How serious

Class II

It could cause temporary or minor harm

Why

See FDA's words below

Status

Terminated

Closed September 5, 2025

The recall

Company
Yerba Prima Inc (Ashland, OR)
Reason, in FDA's words
“Potential contamination with Pseudomonas aeruginosa.”
Where it was sold
Distributed in AZ, CA, CO, CT, FL, GA, IA, IL, IN, KY, MD, MO, NC, NH, NV, NY, OH, PA, TX, VA, and WA.
Recall began
, by the company
FDA classified it
First in an FDA Enforcement Report
FDA event number
97056

The product recalled

As the FDA describes them, with the codes that tell whether a package is part of the recall.

  • H-0050-2025 Class II

    Great Plains Bentonite + Herbal Detox Capsules 60 capsules, packaged in PETE amber bottle, white plastic cap and tamper proof seal. Case GTIN code:100 46352 00518 5. Retail package UPC code: 0 46352 00518 8. Yerba Prima, Inc. 740 Jefferson Ave Ashland, Oregon 97520 USA

    Codes: Lot # 05051, Expiration Date 02/2028. Lot code breaks down as follows: 050 = 3 digits pertaining to the day of the year 5 = last number of the year 2025 1 = number of batch records issued of the day

    Quantity: 4985 bottles

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Source and notes

U.S. Food and Drug Administration, Enforcement Reports (openFDA food recall data) (Public domain (U.S. government work); source U.S. Food and Drug Administration, openFDA), data as of June 25, 2025.

Each week the FDA lists the recalls it has classified in its Enforcement Report, often weeks after the company announced the recall, so a month with five weekly reports tends to count more. Each recall counts once, however many products it covers, in the month FDA first listed it. Class I means the food could cause serious harm or death, Class II temporary or minor harm, and Class III is unlikely to harm anyone. Meat, poultry and most egg products are recalled by the U.S. Department of Agriculture, not the FDA, and aren't included. For what to do with a recalled product, see the FDA's recalls page.