Summary
The FDA issued a Class II for RTB MIXED DANISH Variety by Lecoq Cuisine Corporation. Reason: Contains undeclared soy lecithin..
Details
Source
Food Recall
External ID
F-0787-2024
Action Date
2024-01-31
Status
Terminated
Category
food
Product Description
RTB MIXED DANISH Variety
Lot/Code Info: 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
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-0787-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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