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Food FDA Class II Terminated Pathogen contamination

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

Yerba Prima Inc Published Jun 25, 2025

Risk level

Class II

May cause a temporary or reversible health problem; slight chance of serious harm.

Severity score 50/100

What should you do?

  • Check whether you have this product, using the lot codes, UPCs, and dates listed below.
  • Do not eat, serve, or sell the affected product.
  • Return it to the place of purchase for a refund, or throw it away in a sealed bag so people and animals can’t get to it.
  • Contact Yerba Prima Inc or your place of purchase with questions, and see the source record below for full details.
Reason for recall

Potential contamination with Pseudomonas aeruginosa.

Hazards

Pseudomonas aeruginosa · primary

Affected products (1)

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

4985 bottles

Lot codes: 05051, code
Code info: 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

Affected areas

ArizonaCaliforniaColoradoConnecticutFloridaGeorgiaIllinoisIndianaIowaKentuckyMarylandMissouriNevadaNew HampshireNew YorkNorth CarolinaOhioPennsylvaniaTexasVirginiaWashington

Timeline

  1. Initiated
    Jun 10, 2025
  2. Published
    Jun 25, 2025
  3. Terminated
    Sep 5, 2025
Recall number
H-0050-2025
Agency
U.S. Food and Drug Administration
Country
US
Source data (openFDA JSON) About FDA enforcement reports

FDA records come from the openFDA food enforcement-report dataset — the agency's full weekly enforcement list. Most entries are not issued as consumer press releases, so they won't appear on fda.gov/recalls or in a web search. The source record link above resolves this exact recall by its number.