RecallHawk
Class II Recall

1. 2pc Ganache tote box

Maribel's Sweets, Inc.

Summary

The FDA issued a Class II for 1. 2pc Ganache tote box by Maribel's Sweets, Inc.. Reason: Contains undeclared coconut..

Details

Source

Food Recall

External ID

F-1265-2024

Action Date

2024-06-05

Status

Terminated

Category

food

Product Description

1. 2pc Ganache tote box

Lot/Code Info: Lot/Unit Numbers: 07324,07424, 07824, 07924, 08024, 08124, 08524, 08624, 08724, 08824, 09224, 09324, 08424, 08524, 09924, 10024, 10124, 10224, 10624, 10824, 10724, 10924, 11324, 11424, 11524, 12024, 12124, 12224, 12324 Expiration date(s) or Use by Date(s) or expected shelf life of product: fresh 6 weeks and frozen 1 year UPC Codes: 858289000095

Quantity Affected: 4011 boxes total

Reason for Recall

Contains undeclared coconut.

Distribution

Nationwide E-commerce, retail stores in NY

Type: Voluntary: Firm initiated

Recall Initiated: 2024-05-02

Company

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

Maribel's Sweets, Inc. has 9 FDA actions in our database, including 9 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 (Maribel's Sweets, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Maribel's Sweets, Inc. have FDA actions?

Maribel's Sweets, Inc. has 9 FDA actions in our database, including 9 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-1265-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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