Lecoq Cuisine Corporation Recall: Contains undeclared soy lecithin.

🇺🇸 United States

1. December 15, 2023 - Recall initiated
2. January 31, 2024 - Reported by source
3. July 16, 2024 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-0787-2024

Event ID

93642

Status

Terminated

Classification

Class II

Company

Lecoq Cuisine Corporation

Product description

RTB MIXED DANISH Variety

Quantity

7620 units (total)

Reason

Contains undeclared soy lecithin.

Recall initiation date

December 15, 2023

Report date

January 31, 2024

Classification date

Not published in this source record

Termination date

July 16, 2024

Distribution pattern

Arizona, California, Colorado, Connecticut, Florida, Georgia, Alabama, Indiana, Kansas, Louisiana, Massachusetts, Maryland, Michigan, Minnesota, Missouri, North Carolina, New Jersey, Nevada, New York, Ohio, Pennsylvania, South Carolina, Tennessee, Texas, Utah, Virginia, Wisconsin

UPC, lot, and code information

RDVS-252 Lot Numbers Expiration date 136361 10/25/2023 136664 11/6/2023 136889 11/13/2023 137166 11/21/2023 137693 12/3/2023 137979 12/11/2023 138224 12/17/2023 138550 12/27/2023 138989 1/7/2024 139286 1/15/2024 139548 1/21/2024 139814 1/29/2024 140088 2/6/2024 140499 2/20/2024 141274 3/12/2024 141710 3/27/2024 142342 4/13/2024 142757 4/30/2024 143525 5/29/2024

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 93642 with 1 other product entry in Public Health Trace.

Responsible company: Lecoq Cuisine Corporation

Other recalls from Lecoq Cuisine Corporation

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.

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