RecallHawk
Class II Recall

Montreal Fudge brand Chocolate Fudge with Nuts; 5.6oz

AUTHENTIK FUDGE

Summary

The FDA issued a Class II for Montreal Fudge brand Chocolate Fudge with Nuts; 5.6oz by AUTHENTIK FUDGE. Reason: Product may be contaminated with mold..

Details

Source

Food Recall

External ID

F-1820-2024

Action Date

2024-10-02

Status

Terminated

Category

food

Product Description

Montreal Fudge brand Chocolate Fudge with Nuts; 5.6oz

Lot/Code Info: lot 0241500805 with expiration date of 2025/MR/01, lot 0241690105 with expiration date of 2025/MR/17 lot 0241690205 with expiration date of 2025/MR/17

Quantity Affected: 84 cases of 10 units 840 units total

Reason for Recall

Product may be contaminated with mold.

Distribution

TJ MAXX: Arizona, California, Colorado, New Mexico, Nevada, Utah, Washington, Wyoming MARSHALLS: California, Colorado, Connecticut, Delaware, Florida, Georgia, Iowa, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Michigan, Minnesota, Montana, Mississippi, North Carolina, Nebraska, New Hampshire, New Jersey, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, South Carolina, Tennessee, Texas, Utah, Virginia, Washington, Wisconsin, West Virginia, Wyoming

Type: Voluntary: Firm initiated

Recall Initiated: 2024-08-14

Company

AUTHENTIK FUDGE

Sainte-Julie

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 28 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 (AUTHENTIK FUDGE) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does AUTHENTIK FUDGE have FDA actions?

This is the only FDA action we have on record for AUTHENTIK FUDGE in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-1820-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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