Happy Moose Juice Strawberry Field packaged in a plastic 12 fl. oz. bottle. Ingredients: Organic Apple Juice, Organic Or
Summary
The FDA issued a Class II for Happy Moose Juice Strawberry Field packaged in a plastic 12 fl. oz. bottle. Ingr by Youngstown Grape Distributors, Inc.. Reason: Incomplete pasteurization.
Details
Source
Food Recall
External ID
F-0059-2025
Action Date
2024-10-30
Status
Terminated
Category
food
Product Description
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
Lot/Code Info: Lot: H240903-H; Enjoy by: 12/02/2024
Quantity Affected: 1017 bottles
Reason for Recall
Incomplete pasteurization
Distribution
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
Type: Voluntary: Firm initiated
Recall Initiated: 2024-10-03
Company
Reedley, CA
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 42 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Youngstown Grape Distributors, Inc. has 5 FDA actions in our database, including 5 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Youngstown Grape Distributors, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Youngstown Grape Distributors, Inc. have FDA actions?
Youngstown Grape Distributors, Inc. has 5 FDA actions in our database, including 5 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0059-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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