Summary
The FDA issued a Class II for R&B Chocolate Chips Croissant Twist by Lecoq Cuisine Corporation. Reason: Contains undeclared soy lecithin..
Details
Source
Food Recall
External ID
F-0786-2024
Action Date
2024-01-31
Status
Terminated
Category
food
Product Description
R&B Chocolate Chips Croissant Twist
Lot/Code Info: 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
Quantity Affected: 7620 units (total)
Reason for Recall
Contains undeclared soy lecithin.
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
Type: Voluntary: Firm initiated
Recall Initiated: 2023-12-15
Company
Bridgeport, CT
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 85 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Lecoq Cuisine Corporation has 2 FDA actions in our database, including 2 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 (Lecoq Cuisine Corporation) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Lecoq Cuisine Corporation have FDA actions?
Lecoq Cuisine Corporation has 2 FDA actions in our database, including 2 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0786-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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