The Coastal Companies DBA Hearn Kirkwood Recall: Undeclared milk and soy

🇺🇸 United States

1. November 3, 2023 - Recall initiated
2. December 6, 2023 - Reported by source
3. September 25, 2024 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-0475-2024

Event ID

93386

Status

Terminated

Classification

Class II

Company

The Coastal Companies DBA Hearn Kirkwood

Product description

Le Croissant Turkey & Cheddar Net Wt. 5.5oz (156g) UPC:766375261629 Packaged in clamshell container. Sold as single unit and 6-unit pack under Food Unlimited brand

Quantity

238 clamshells

Reason

Undeclared milk and soy

Recall initiation date

November 3, 2023

Report date

December 6, 2023

Classification date

Not published in this source record

Termination date

September 25, 2024

Distribution pattern

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

UPC, lot, and code information

UPC 766375261629; Use By Date of 10/27/2023 through 11/8/2023

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Source last updated

Not tracked separately from the Public Health Trace retrieval date below

Public Health Trace retrieval date

July 18, 2026 ET

Other products recalled under this same event

This recall shares FDA event ID 93386 with 4 other product entries in Public Health Trace.

Responsible company: The Coastal Companies DBA Hearn Kirkwood

Other recalls from The Coastal Companies DBA Hearn Kirkwood

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace: July 18, 2026 ET

Frequently asked questions

What does a Class II mean?

A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.

• Email
• X / Twitter
• Facebook