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RECALL RECORD — CLASS IIIRecall closedF-0044-2017/FDA enforcement
Kracker Enterprises, LLC·Food·Apr 29, 2016

Doctor Kracker Klassic 3 Seed Crispbreads NET WT 7 OZ (200g) in Cardboard Container

What you need to know

Class III

  • What happened

    Milk declared in the ingredient statement although the product does not contain milk.

  • Health risk

    The product is unlikely to cause adverse health consequences. These recalls are often related to labeling or quality violations. 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 FDACA, IA, IL, MD +6 moreMore food

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Match before you discard

Product identification

Source: FDA FOOD

Brand nameKracker Enterprises, LLC
Recalling firmKracker Enterprises, LLCPlano, TX, United States
UPC / barcodes
1 70189 11605 41 70111 11606 01 70114 41606 71 70114 41607 41 70117 61607 41 70120 71608 2
Lot / date codes
  • Lot Number: 170189116054, 170111116060, 170114416067, 170114416074, 170117616074, 170120716082
Distribution area
CAIAILMDMONYRITXWAWI

CA, IA, IL, MD, MO, NY, RI, TX, WA, WI

United States

Quantity affected9951 cases
Recall initiationFDA report date: October 19, 2016
FDA recall numberF-0044-2017

Beyond the headline

The recall, in context

Kracker Enterprises, LLC initiated this food recall on April 29, 2016. The FDA enforcement report states: Milk declared in the ingredient statement although the product does not contain milk. The FDA report lists distribution as: CA, IA, IL, MD, MO, NY, RI, TX, WA, WI.

The FDA enforcement report describes the reason as: Milk declared in the ingredient statement although the product does not contain milk.

Doctor Kracker Klassic 3 Seed Crispbreads NET WT 7 OZ (200g) in Cardboard Container was made or distributed by Kracker Enterprises, LLC in Plano, TX, United States. This page reflects FDA report F-0044-2017, dated October 19, 2016.

Why this is a Class III recall

Class III means the product is unlikely to cause adverse health consequences. These recalls are often related to labeling or quality violations. In this recall, a safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.

FDA definition

The product is unlikely to cause adverse health consequences. These recalls are often related to labeling or quality violations.

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 milk

Symptoms to watch for

Hives, swelling, wheezing, vomiting or anaphylaxis can occur in people with a milk 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 cow's milk allergy, especially children and anyone with a history of anaphylaxis.

What to do now

  1. 1Do not eat the product if you have a milk 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 Doctor Kracker Klassic 3 Seed Crispbreads NET WT 7 OZ (200g) in Cardboard Container recall?

Kracker Enterprises, LLC recalled Doctor Kracker Klassic 3 Seed Crispbreads NET WT 7 OZ (200g) in Cardboard Container in an FDA Class III enforcement action reported as F-0044-2017. Milk declared in the ingredient statement although the product does not contain milk.

What are the symptoms of Undeclared milk exposure?

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

How quickly can Undeclared milk symptoms appear?

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

Who is most at risk from Undeclared milk?

People with a diagnosed cow's milk 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 milk 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 Kracker Enterprises, 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-0044-2017 and keep the packaging, lot code and proof of purchase if you have them.

Is the Kracker Enterprises, 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-0044-2017. 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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Kracker Enterprises, LLC

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