RECALL RECORD — CLASS IIRecall closedF-0280-2021/FDA enforcement

Buffalo Style Chicken Sliders NET WT

What you need to know

Class II
  • What happened

    The firm was notified by a customer that the Buffalo Style Chicken Sliders contain the ingredient panel for their Tuna Salad Croissants. The label does not included Soy in the…

  • Health risk

    The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. A safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.

  • Action required

    Check the identifying codes below and stop using the product. Return it to the retailer for a refund or dispose of it safely, following the recall notice.

Recall closed · classified by the FDAAL, GA, SCMore food

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Product identification

Source: FDA FOOD

Brand nameRenaissance Food Group LLC
Recalling firmRenaissance Food Group, LLCRancho Cordova, CA, United States
UPC / barcodes
8 26766 15590 3
Lot / date codes
  • Sell By: 01/29/21 GHGA 024
Distribution area
ALGASC

Product was shipped to the following states: AL, GA, SC.

United States

Quantity affected226/5 oz. packages
Recall initiationFDA report date: February 17, 2021
FDA recall numberF-0280-2021

Beyond the headline

The recall, in context

Renaissance Food Group, LLC initiated this food recall on January 29, 2021. The FDA enforcement report states: The firm was notified by a customer that the Buffalo Style Chicken Sliders contain the ingredient panel for their Tuna Salad Croissants. The label does not included Soy in the Contain statement. The FDA report lists distribution as: Product was shipped to the following states: AL, GA, SC.

The FDA enforcement report describes the reason as: The firm was notified by a customer that the Buffalo Style Chicken Sliders contain the ingredient panel for their Tuna Salad Croissants. The label does not included Soy in the Contain statement.

Buffalo Style Chicken Sliders NET WT was made or distributed by Renaissance Food Group, LLC in Rancho Cordova, CA, United States. This page reflects FDA report F-0280-2021, dated February 17, 2021.

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, a safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.

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 Buffalo Style Chicken Sliders NET WT recall?

Renaissance Food Group LLC recalled Buffalo Style Chicken Sliders NET WT in an FDA Class II enforcement action reported as F-0280-2021. The firm was notified by a customer that the Buffalo Style Chicken Sliders contain the ingredient panel for their Tuna Salad Croissants. The label does not included Soy in the…

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?

Check the identifying codes below and stop using the product. Return it to the retailer for a refund or dispose of it safely, following the recall notice. 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 Renaissance Food Group LLC?

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-0280-2021 and keep the packaging, lot code and proof of purchase if you have them.

Is the Renaissance Food Group LLC 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-0280-2021. 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.