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Lecoq Cuisine Corporation Recall: Contains undeclared soy lecithin.

United States

TerminatedClass II

Company
Lecoq Cuisine Corporation
Product
R&B Chocolate Chips Croissant Twist
Recall date
December 15, 2023
Terminated
July 16, 2024
Source
FDA

Reason for recall

Contains undeclared soy lecithin.

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
R&B Chocolate Chips Croissant Twist Not published in this source record 7620 units (total) Model, catalog, or product order numbers: RTCHOL-96, RTCHOL-96C Lot Expiration Date 135823 10/14/2023 135903 10/19/2023 136097 10/25/2023 136417 11/2/2023 136707 11/9/2023 136914 11/15/2023 137178 11/22/2023 137417 11/27/2023 137723 12/5/2023 137968 12/10/2023 138281 12/21/2023 138355 12/19/2023 138974 1/6/2024 139028 1/10/2024 139842 1/30/2024 140347 2/15/2024 141039 3/5/2024 141263 3/11/2024 141459 3/19/2024 141686 3/25/2024 142148 4/8/2024 142551 4/21/2024 142716 4/27/2024 142905 5/4/2024 142935 5/6/2024 143113 5/13/2024 143123 5/14/2024 143138 5/14/2024 143312 5/18/2024 143527 5/29/2024 143714 6/1/2024 143728 6/2/2024 143736 6/3/2024 143746 6/4/2024 143762 6/5/2024 143849 6/8/2024

Distribution

  • 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

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-0786-2024
Event ID
93642
Status
Terminated
Classification
Class II
Company
Lecoq Cuisine Corporation
Product description
R&B Chocolate Chips Croissant Twist
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
Model, catalog, or product order numbers: RTCHOL-96, RTCHOL-96C Lot Expiration Date 135823 10/14/2023 135903 10/19/2023 136097 10/25/2023 136417 11/2/2023 136707 11/9/2023 136914 11/15/2023 137178 11/22/2023 137417 11/27/2023 137723 12/5/2023 137968 12/10/2023 138281 12/21/2023 138355 12/19/2023 138974 1/6/2024 139028 1/10/2024 139842 1/30/2024 140347 2/15/2024 141039 3/5/2024 141263 3/11/2024 141459 3/19/2024 141686 3/25/2024 142148 4/8/2024 142551 4/21/2024 142716 4/27/2024 142905 5/4/2024 142935 5/6/2024 143113 5/13/2024 143123 5/14/2024 143138 5/14/2024 143312 5/18/2024 143527 5/29/2024 143714 6/1/2024 143728 6/2/2024 143736 6/3/2024 143746 6/4/2024 143762 6/5/2024 143849 6/8/2024
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

Other products recalled under this same event

This recall shares FDA event ID 93642 with 1 other product entry in Public Health Trace.

FDA Recall United States Terminated Historical recordClass II

Lecoq Cuisine Corporation

Product
RTB MIXED DANISH Variety
Published
January 31, 2024
Distribution
Arizona, California, Colorado, Connectic…

View recall →

Responsible company: Lecoq Cuisine Corporation

Other recalls from Lecoq Cuisine Corporation

FDA Recall United States Terminated Historical recordClass II

Lecoq Cuisine Corporation

Product
RTB MIXED DANISH Variety
Published
January 31, 2024
Distribution
Arizona, California, Colorado, Connectic…

View recall →

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:

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.