RecallHawk
Class II Recall

Assorted Chocolate Caramels with kosher sea salt, Net Weight 1.25lb

V Chocolates, Inc

Summary

The FDA issued a Class II for Assorted Chocolate Caramels with kosher sea salt, Net Weight 1.25lb by V Chocolates, Inc. Reason: Small pieces of plastic broken tray in the product..

Details

Source

Food Recall

External ID

F-0580-2025

Action Date

2025-03-05

Status

Terminated

Category

food

Product Description

Assorted Chocolate Caramels with kosher sea salt, Net Weight 1.25lb

Lot/Code Info: lot code# 27424, best by date: April 1, 2024

Quantity Affected: 60-1.25 lb boxes of 32 count chocolate candy caramels

Reason for Recall

Small pieces of plastic broken tray in the product.

Distribution

Distributed nationwide within the United States.

Type: Voluntary: Firm initiated

Recall Initiated: 2024-12-30

Company

V Chocolates, Inc

Salt Lake Cty, UT

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 20 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 (V Chocolates, Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does V Chocolates, Inc have FDA actions?

This is the only FDA action we have on record for V Chocolates, Inc in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0580-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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