RecallHawk
Class II Recall

Happy Moose Juice Tropical Roots packaged in a plastic 12 fl. oz. bottle. Ingredients: Mandarin Orange, Organic Carrot J

Youngstown Grape Distributors, Inc.

Summary

The FDA issued a Class II for Happy Moose Juice Tropical Roots packaged in a plastic 12 fl. oz. bottle. Ingred by Youngstown Grape Distributors, Inc.. Reason: Incomplete pasteurization.

Details

Source

Food Recall

External ID

F-0058-2025

Action Date

2024-10-30

Status

Terminated

Category

food

Product Description

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

Lot/Code Info: Lot: H240903-E; Enjoy by: 12/02/2024

Quantity Affected: 1701 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

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-0058-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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