CLASS II Food recall · Reported 25 Jun 2025 · FDA Enforcement Report
Great Plains Bentonite + Herbal Detox Capsules recalled by Yerba Prima
Yerba Prima is recalling Great Plains Bentonite + Herbal Detox Capsules, distributed in 21 states. The recall was initiated on 10 Jun 2025 and the FDA has classified it as Class II.
Check your package
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
Recall details
- Recall number
- H-0050-2025
- FDA event ID
- 97056
- Recalling firm
- Yerba Prima, Ashland, OR
- Brand
- Great Plains
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 10 Jun 2025
- FDA classified
- 17 Jun 2025
- Reported
- 25 Jun 2025
- Type
- Voluntary: Firm initiated
- Customers notified by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Reason category
- Sterility
- Product category
- Herbal Supplements
Timeline
| 10 Jun 2025 | Recall initiated by company | |
| 17 Jun 2025 | Classified by FDA | +7 days |
| 25 Jun 2025 | Published in enforcement report | +8 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Potential contamination with Pseudomonas aeruginosa.
A sterility recall means a product that must be sterile, such as an injection or eye drop, may be contaminated. Using a non-sterile product can cause serious infection.
Product as listed by the FDA
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
Where it was distributed
Distributed in AZ, CA, CO, CT, FL, GA, IA, IL, IN, KY, MD, MO, NC, NH, NV, NY, OH, PA, TX, VA, and WA.
ArizonaCaliforniaColoradoConnecticutFloridaGeorgiaIowaIllinoisIndianaKentuckyMarylandMissouriNorth CarolinaNew HampshireNevadaNew YorkOhioPennsylvaniaTexasVirginia
Questions about this recall
Why was it recalled?
Potential contamination with Pseudomonas aeruginosa.
Which lots are affected?
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
Where was it 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.
What should I do if I have it?
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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