Food Recall Check
Class II · Moderate risk Terminated Initiated Oct 3, 2024 (2 years ago)

Farmers Juice Carrot Digest packaged in a recall

Recalled by Youngstown Grape Distributors, Inc. · Reedley, CA, United States

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

Why it was recalled

Incomplete pasteurization

These are failures of the safety steps that keep food safe - cooking, pasteurising, keeping cold, sealing - even when no contaminant has yet been found. All processing & sanitation problems recalls.

What was recalled

Farmers Juice Carrot Digest packaged in a 12 fl. oz. bottle; Ingredients: Orange, Lemon, Carrot, Ginger, Jicama UPC: 00860006798116

Quantity: 2521 bottles

Food: Juice & beverages

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 Number: H240930-E (This is not printed on the bottle); Enjoy by: 12/29/2024

Where it was sold

Alabama Arizona California Colorado Connecticut Florida Georgia Iowa Idaho Illinois Indiana Kansas Kentucky Louisiana Massachusetts Maryland Maine Michigan Minnesota Missouri North Carolina North Dakota Nebraska New Jersey New Mexico Nevada New York Ohio Oklahoma Oregon Pennsylvania Rhode Island South Carolina Tennessee Texas Utah Virginia Washington Wisconsin

FDA's distribution note: CA, TX, WA, KY, NC, NY, IL, VA, AL, GA, KS, CT, MI, MA, PA, OH, MD, WI, ND, MO, TN, NE, KS, RI, MN, FL, SC, IN, NJ, IA, OK, LA, TN, ME, UT, CA, OR, CO, WA, AZ, NM, ID, and NV

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
Youngstown Grape Distributors, Inc.
Initiated by
Voluntary: Firm initiated
Recall initiated
Oct 3, 2024
In FDA report of
Oct 30, 2024
Terminated
Apr 14, 2025
FDA recall number
F-0061-2025 · event 95488
Official record
FDA enforcement report search

Also recalled with it (4 more products)

FDA files each product of one recall action separately; these share the same FDA event.

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