RecallHawk
Class II Recall

Le Croissant Ham & Swiss Net Wt. 5.5oz (156g) UPC:766375261612 Packaged in clamshell container. Sold under Food Unlimite

The Coastal Companies DBA Hearn Kirkwood

Summary

The FDA issued a Class II for Le Croissant Ham & Swiss Net Wt. 5.5oz (156g) UPC:766375261612 Packaged in clams by The Coastal Companies DBA Hearn Kirkwood. Reason: Undeclared milk and soy.

Details

Source

Food Recall

External ID

F-0474-2024

Action Date

2023-12-06

Status

Terminated

Category

food

Product Description

Le Croissant Ham & Swiss Net Wt. 5.5oz (156g) UPC:766375261612 Packaged in clamshell container. Sold under Food Unlimited brand.

Lot/Code Info: Use By Date of 10/27/2023 through 11/8/2023

Quantity Affected: 108 clamshells

Reason for Recall

Undeclared milk and soy

Distribution

Distributed to consignees in Alabama, Connecticut, Washington, D.C., Delaware, Florida, Georgia, Kentucky, Maryland, Michigan, North Carolina, Ohio, Pennsylvania, Tennessee, Virginia, and West Virginia.

Type: Voluntary: Firm initiated

Recall Initiated: 2023-11-03

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

The Coastal Companies DBA Hearn Kirkwood has 7 FDA actions in our database, including 7 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 (The Coastal Companies DBA Hearn Kirkwood) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does The Coastal Companies DBA Hearn Kirkwood have FDA actions?

The Coastal Companies DBA Hearn Kirkwood has 7 FDA actions in our database, including 7 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0474-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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