Food Recall Check
Class II · Moderate risk Terminated Initiated Jun 10, 2025 (16 months ago)

Great Plains Bentonite + Herbal Detox Capsules 60 capsules recall

Recalled by Yerba Prima Inc · Ashland, OR, United States

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Potential contamination with Pseudomonas aeruginosa.

See the recall's own reason text for the specifics. All other reasons recalls.

What was recalled

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

Quantity: 4985 bottles

Food: Dietary supplements

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

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 it was sold

Arizona California Colorado Connecticut Florida Georgia Iowa Illinois Indiana Kentucky Maryland Missouri North Carolina New Hampshire Nevada New York Ohio Pennsylvania Texas Virginia Washington

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

Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm
Yerba Prima Inc
Initiated by
Voluntary: Firm initiated
Recall initiated
Jun 10, 2025
In FDA report of
Jun 25, 2025
Terminated
Sep 5, 2025
FDA recall number
H-0050-2025 · event 97056
Official record
FDA enforcement report search

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