Class II Recall

FULL CIRCLE market COCONUTMILK CHOCOLATE ALMOND CRUNCH NON0DAIRY FROZEN DESSERT 16 FLOZ (1PT) 473 mL UPC 0 36800 46964 8

Summary

The FDA issued a Class II for FULL CIRCLE market COCONUTMILK CHOCOLATE ALMOND CRUNCH NON0DAIRY FROZEN DESSERT by G.S. Gelato and Desserts Inc.. Reason: Undeclared cashews. The firm was notified by a customer that the top label and the carton labels do not match. The carton label states, "coconut milk".

Details

Source

Food Recall

External ID

F-1702-2024

Action Date

2024-08-21

Status

Terminated

Product Description

FULL CIRCLE market COCONUTMILK CHOCOLATE ALMOND CRUNCH NON0DAIRY FROZEN DESSERT 16 FLOZ (1PT) 473 mL UPC 0 36800 46964 8 DISTRIBUTED BY TOPCO ASSOCIATES LLC ELK GROVE VILLAGE, IL 60007

Lot/Code Info: FL LIC 1601 LOT 041624L2 BBD 10/15/2025

Quantity Affected: 1,080cs/8/1pt containers

Reason for Recall

Undeclared cashews. The firm was notified by a customer that the top label and the carton labels do not match. The carton label states, "coconut milk" while the top label states, "cashew milk". The product actually contains the cashew milk product.

Distribution

The product was shipped to the following states: GA, MA & NY.

Type: Voluntary: Firm initiated

Recall Initiated: 2024-07-24

Company

G.S. Gelato and Desserts Inc.

Fort Walton Beach, FL

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 125 food recalls issued in the same week, part of 204 food-related FDA actions this month.

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 (G.S. Gelato and Desserts Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does G.S. Gelato and Desserts Inc. have FDA actions?

This is the only FDA action we have on record for G.S. Gelato and Desserts Inc. in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-1702-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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