RecallHawk
Class II Recall

RTB MIXED DANISH Variety

Lecoq Cuisine Corporation

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

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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