RecallHawk
Class II Recall

Neiman Marcus Christmas Petit Fours 24pc

Sweet Shop Candies, Inc

Summary

The FDA issued a Class II for Neiman Marcus Christmas Petit Fours 24pc by Sweet Shop Candies, Inc. Reason: mold and yeast in product.

Details

Source

Food Recall

External ID

F-0774-2024

Action Date

2024-01-24

Status

Terminated

Category

food

Product Description

Neiman Marcus Christmas Petit Fours 24pc

Lot/Code Info: 33050163

Quantity Affected: 1488 units

Reason for Recall

mold and yeast in product

Distribution

Product was distributed to one distribution center. Then to retail stores in TX, PA, CA, MO, IL, VA, NC, NJ, FL, CO, GA, NY, NV, MA, MI, HI, AZ

Type: Voluntary: Firm initiated

Recall Initiated: 2023-12-08

Company

Sweet Shop Candies, Inc

Mount Pleasant, TX

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 81 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 (Sweet Shop Candies, Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Sweet Shop Candies, Inc have FDA actions?

This is the only FDA action we have on record for Sweet Shop Candies, Inc in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0774-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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