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RECALL RECORD — CLASS IRecall closedF-3558-2017/FDA enforcement
Dierbergs Markets, INC Corporate Office·Food·Aug 14, 2017

Scampi Butter, NET WT

What you need to know

Class I

  • What happened

    Flavored butter contains undeclared fish (bonito and cod) and crustacean shellfish (shrimp, crab, and lobster).

  • Health risk

    The product has a reasonable probability of causing serious adverse health consequences or death. Fish-derived ingredients were omitted from the label, creating a risk for fish-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 FDAINMore food

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Product identification

Source: FDA FOOD

Brand nameDierbergs Markets, INC Corporate Office
Recalling firmDierbergs Markets, INC Corporate OfficeChesterfield, MO, United States
UPC / barcodesNo UPC listed in the FDA enforcement record.
Lot / date codes
  • Sell-by dates 10/9/17 and earlier.
Distribution area
IN

Distributed to retail grocery stores in central and western Missouri and eastern Illinois.

United States

Quantity affected1, 242 3 oz containers
Recall initiationFDA report date: September 27, 2017
FDA recall numberF-3558-2017

Beyond the headline

The recall, in context

Dierbergs Markets, INC Corporate Office initiated this food recall on August 14, 2017. The FDA enforcement report states: Flavored butter contains undeclared fish (bonito and cod) and crustacean shellfish (shrimp, crab, and lobster). The FDA report lists distribution as: Distributed to retail grocery stores in central and western Missouri and eastern Illinois.

The FDA enforcement report describes the reason as: Flavored butter contains undeclared fish (bonito and cod) and crustacean shellfish (shrimp, crab, and lobster).

Scampi Butter, NET WT was made or distributed by Dierbergs Markets, INC Corporate Office in Chesterfield, MO, United States. This page reflects FDA report F-3558-2017, dated September 27, 2017.

Why this is a Class I recall

Class I means the product has a reasonable probability of causing serious adverse health consequences or death. 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 has a reasonable probability of causing serious adverse health consequences or death.

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 lot and date codes 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 fish

Symptoms to watch for

Hives, swelling, wheezing, vomiting or anaphylaxis can occur in people with a fish 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 fish allergy, especially anyone with a history of anaphylaxis.

What to do now

  1. 1Do not eat the product if you have a fish 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 Scampi Butter, NET WT recall?

Dierbergs Markets, INC Corporate Office recalled Scampi Butter, NET WT in an FDA Class I enforcement action reported as F-3558-2017. Flavored butter contains undeclared fish (bonito and cod) and crustacean shellfish (shrimp, crab, and lobster).

What are the symptoms of Undeclared fish exposure?

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

How quickly can Undeclared fish symptoms appear?

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

Who is most at risk from Undeclared fish?

People with a diagnosed fish allergy, especially 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 fish 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 Dierbergs Markets, INC Corporate Office?

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-3558-2017 and keep the packaging, lot code and proof of purchase if you have them.

Is the Dierbergs Markets, INC Corporate Office 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-3558-2017. 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.