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RECALL RECORD — CLASS IIRecall closedH-0050-2025/FDA enforcement
Yerba Prima INC·Food·Jun 10, 2025

Great Plains Bentonite + Herbal Detox Capsules 60 Capsules, Packaged in Pete Amber Bottle, …

What you need to know

Class II

  • What happened

    Potential contamination with Pseudomonas aeruginosa.

  • Health risk

    The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. A safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.

  • Action required

    Check the identifying codes below and stop using the product. Return it to the retailer for a refund or dispose of it safely, following the recall notice.

Recall closed · classified by the FDAIN, AZ, CA, CO +17 moreMore food

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Match before you discard

Product identification

Source: FDA FOOD

Brand nameYerba Prima INC
Recalling firmYerba Prima INCAshland, OR, United States
UPC / barcodes
10 046352 00518 50 46352 00518 8
Lot / date 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
Distribution area
INAZCACOCTFLGAIAILKYMDMONCNHNVNYOHPATXVAWA

Distributed in AZ, CA, CO, CT, FL, GA, IA, IL, IN, KY, MD, MO, NC, NH, NV, NY, OH, PA, TX, VA, and WA.

United States

Quantity affected4985 bottles
Recall initiationFDA report date: June 25, 2025
FDA recall numberH-0050-2025

Beyond the headline

The recall, in context

Yerba Prima INC initiated this food recall on June 10, 2025. The FDA enforcement report states: Potential contamination with Pseudomonas aeruginosa. The FDA report lists distribution as: Distributed in AZ, CA, CO, CT, FL, GA, IA, IL, IN, KY, MD, MO, NC, NH, NV, NY, OH, PA, TX, VA, and WA.

The FDA enforcement report describes the reason as: Potential contamination with Pseudomonas aeruginosa.

Great Plains Bentonite + Herbal Detox Capsules 60 Capsules, Packaged in Pete Amber Bottle, … was made or distributed by Yerba Prima INC in Ashland, OR, United States. This page reflects FDA report H-0050-2025, dated June 25, 2025.

Why this is a Class II recall

Class II means the product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. In this recall, a safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.

FDA definition

The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote.

What to do now

  1. 1

    Stop using it

    Do not eat, drink or take the affected product.

  2. 2

    Check the codes

    Compare the UPC and lot code against the table above.

  3. 3

    Return or discard

    Contact the retailer or recalling firm about a refund, and dispose of the product safely.

Consumer safety guide

Product safety recall

Symptoms to watch for

The official enforcement report describes the specific risk. Follow the recall notice, check the product codes and do not use a product that may be affected.

Higher-risk groups

Children, pregnant people, older adults and people with weakened immune systems should take extra care when a product's safety is uncertain.

What to do now

  1. 1Stop using or eating the product and keep it away from children and pets.
  2. 2Check the UPC and lot/date codes on this page and follow the official recall notice for disposal or return.
  3. 3Seek medical advice if anyone develops severe or worrying symptoms after exposure.

Read the official source record for the specific hazard and instructions.

This is general consumer safety information, not medical advice or a diagnosis. Follow the official recall notice and contact a healthcare professional if you have concerns about exposure or symptoms.

Frequently asked

Questions about this recall

What is the Great Plains Bentonite + Herbal Detox Capsules 60 Capsules, Packaged in Pete Amber Bottle, … recall?

Yerba Prima INC recalled Great Plains Bentonite + Herbal Detox Capsules 60 Capsules, Packaged in Pete Amber Bottle, … in an FDA Class II enforcement action reported as H-0050-2025. Potential contamination with Pseudomonas aeruginosa.

What should I do if I bought this product?

Check the identifying codes below and stop using the product. Return it to the retailer for a refund or dispose of it safely, following the recall notice. Stop using or eating the product and keep it away from children and pets. Check the UPC and lot/date codes on this page and follow the official recall notice for disposal or return. Seek medical advice if anyone develops severe or worrying symptoms after exposure.

Is the Yerba Prima INC recall still active?

The FDA lists this recall as recall closed. It remains relevant if you still have the affected product or need to identify a historical recall.

Where can I verify this recall?

This page is normalized from the openFDA enforcement record H-0050-2025. You can verify it directly using the official source link on this page. VerifyRecall updates its index from public FDA enforcement data and does not replace advice from the FDA, the recalling firm or a healthcare professional.

Verify before you act.

VerifyRecall is independent and not affiliated with the FDA. Always confirm the latest status on the official source record.

Official source

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Record last synced from official openFDA enforcement data on November 14, 2026. Source record: official FDA notice.