Class IIPossible risk
Farmers Juice: Juice beverages
Incomplete pasteurization
5 recalled products
Happy Moose Juice Tropical Roots packaged in a plastic 12 fl. oz. bottle. Ingredients: Mandarin Orange, Organic Carrot Juice, Organic Pineapple Juice, Lemon Juice, and Organic Turmeric Juice. UPC 860012096503
Codes on the package: Lot: H240903-E; Enjoy by: 12/02/2024
Happy Moose Juice Strawberry Field packaged in a plastic 12 fl. oz. bottle. Ingredients: Organic Apple Juice, Organic Orange Juice, Organic Strawberry Puree, Organic Beet Juice, Organic Ginger Juice, Organic Turmeric Juice, Organic Goji Berry Powder, and Organic Cayenne Pepper. UPC 86617500388
Codes on the package: Lot: H240903-H; Enjoy by: 12/02/2024
Farmers Juice Focus Greens packaged in a 12 fl. oz. bottle; Ingredients: Cucumber, Celery, Fennel, Romaine Lettuce, Lemon, Mint, Green Cabbage, Ginger, Turmeric, Basil, & Matcha. UPC: 00860006798048
Codes on the package: Lot Number H240906-G (This is not printed on the bottle); Enjoy By: 12/05/2024
Farmers Juice Carrot Digest packaged in a 12 fl. oz. bottle; Ingredients: Orange, Lemon, Carrot, Ginger, Jicama UPC: 00860006798116
Codes on the package: Lot Number: H240930-E (This is not printed on the bottle); Enjoy by: 12/29/2024
Farmers Juice Watermelon Hydration packaged in a 12 fl. oz. bottle; Ingredients: Watermelon, Lime, Mint
Codes on the package: Lot Number H240930-C (This is not printed on the bottle); Enjoy by: 12/29/2024
This recall is no longer in progress, but product already in your home is still recalled. If you have this product, don’t eat it or feed it. Throw it away, or return it where you bought it.
- Status
- Closed by the FDA (Terminated)
- Type
- Food
- Recalled by
- Youngstown Grape Distributors, Inc.
- Posted by the FDA
- Started by the firm
- Classified
- Sold in
- 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
From the FDA
This recall is in the FDA’s Enforcement Report under recall numbers F-0058-2025, F-0059-2025, F-0060-2025, F-0061-2025, F-0062-2025. The headline above is a summary; the product descriptions are the FDA’s own words.