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RECALL RECORD — CLASS IIRecall closedF-0787-2024/FDA enforcement
Lecoq Cuisine Corporation·Food·Dec 15, 2023

Rtb Mixed Danish Variety

What you need to know

Class II

  • What happened

    Contains undeclared soy lecithin.

  • Health risk

    The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. An allergen that is present but missing or incorrect on the label can cause a serious reaction in allergic consumers.

  • Action required

    Do not eat the product if you or someone in your household has a diagnosed allergy. Check the codes below, return it to the retailer for a refund, or dispose of it safely. Seek urgent care for signs of a severe allergic reaction.

Recall closed · classified by the FDADistribution not listedMore food

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Product identification

Source: FDA FOOD

Brand nameLecoq Cuisine Corporation
Recalling firmLecoq Cuisine CorporationBridgeport, CT, United States
UPC / barcodes
2 02313 66641 12 02313 68891 12 02313 71661 12 02313 76931 22 02313 79791 22 02313 82241 22 02313 85501 2
Lot / date codes
  • 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
Distribution area

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

United States

Quantity affected7620 units (total)
Recall initiationFDA report date: January 31, 2024
FDA recall numberF-0787-2024

Beyond the headline

The recall, in context

Lecoq Cuisine Corporation initiated this food recall on December 15, 2023. The FDA enforcement report states: Contains undeclared soy lecithin. The FDA report lists distribution as: 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.

The FDA enforcement report describes the reason as: Contains undeclared soy lecithin.

Rtb Mixed Danish Variety was made or distributed by Lecoq Cuisine Corporation in Bridgeport, CT, United States. This page reflects FDA report F-0787-2024, dated January 31, 2024.

Why this is a Class II recall

Class II means the product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. In this recall, an allergen that is present but missing or incorrect on the label can cause a serious reaction in allergic consumers.

FDA definition

The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote.

What to do now

  1. 1

    Stop using it

    Do not eat, drink or take the affected product.

  2. 2

    Check the codes

    Compare the UPC and lot code against the table above.

  3. 3

    Return or discard

    Contact the retailer or recalling firm about a refund, and dispose of the product safely.

Consumer safety guide

Undeclared soy

Symptoms to watch for

Hives, swelling, wheezing, vomiting or anaphylaxis can occur in people with a soy allergy.

When symptoms may appear

Reactions can begin within minutes to a few hours after eating the product.

Higher-risk groups

People with a diagnosed soy allergy, especially children and anyone with a history of anaphylaxis.

What to do now

  1. 1Do not eat the product if you have a soy allergy.
  2. 2Seek emergency care for breathing difficulty, throat swelling or other signs of anaphylaxis.
  3. 3Keep the packaging and contact the retailer or manufacturer about a refund.

This is general consumer safety information, not medical advice or a diagnosis. Follow the official recall notice and contact a healthcare professional if you have concerns about exposure or symptoms.

Frequently asked

Questions about this recall

What is the Rtb Mixed Danish Variety recall?

Lecoq Cuisine Corporation recalled Rtb Mixed Danish Variety in an FDA Class II enforcement action reported as F-0787-2024. Contains undeclared soy lecithin.

What are the symptoms of Undeclared soy exposure?

Hives, swelling, wheezing, vomiting or anaphylaxis can occur in people with a soy allergy.

How quickly can Undeclared soy symptoms appear?

Reactions can begin within minutes to a few hours after eating the product.

Who is most at risk from Undeclared soy?

People with a diagnosed soy allergy, especially children and anyone with a history of anaphylaxis.

What should I do if I bought this product?

Do not eat the product if you or someone in your household has a diagnosed allergy. Check the codes below, return it to the retailer for a refund, or dispose of it safely. Seek urgent care for signs of a severe allergic reaction. Do not eat the product if you have a soy allergy. Seek emergency care for breathing difficulty, throat swelling or other signs of anaphylaxis. Keep the packaging and contact the retailer or manufacturer about a refund.

How do I get a refund from Lecoq Cuisine Corporation?

Contact the recalling company or the retailer where you purchased the product, quote the FDA recall number and ask about a refund or replacement. Keep the packaging, lot code and proof of purchase where possible. The FDA does not issue consumer refunds. Reference FDA recall F-0787-2024 and keep the packaging, lot code and proof of purchase if you have them.

Is the Lecoq Cuisine Corporation recall still active?

The FDA lists this recall as recall closed. It remains relevant if you still have the affected product or need to identify a historical recall.

Where can I verify this recall?

This page is normalized from the openFDA enforcement record F-0787-2024. You can verify it directly using the official source link on this page. VerifyRecall updates its index from public FDA enforcement data and does not replace advice from the FDA, the recalling firm or a healthcare professional.

Verify before you act.

VerifyRecall is independent and not affiliated with the FDA. Always confirm the latest status on the official source record.

Official source

Brand history

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Record last synced from official openFDA enforcement data on November 14, 2026. Source record: official FDA notice.