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ACTIVE RECALL — CLASS IIActive recallF-0688-2024/FDA enforcement
Carolina Copacking, LLC·Food·Dec 13, 2023

Scratch Pasta Co Marinara Sauce NET WT

What you need to know

Class II

  • What happened

    During a contract inspection by the North Carolina Department of Agriculture, NCDA, informed the firm that the labeling does not list the common name of "milk".

  • 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.

Active recall · classified by the FDAIN, VAMore food

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Product identification

Source: FDA FOOD

Brand nameCarolina Copacking, LLC
Recalling firmCarolina Copacking, LLCHenderson, NC, United States
UPC / barcodes
8 50053 68700 6
Lot / date codes
  • Lot #'s: 2C0470223 BEST BY 02/25, 1C1880723 BEST BY 07/25, AND 2C1930723 BEST BY 07/25
Distribution area
INVA

Product was shipped to one customer in VA

United States

Quantity affected304 cases/6/24.5 oz glass jars
Recall initiationFDA report date: January 10, 2024
FDA recall numberF-0688-2024

Beyond the headline

The recall, in context

Carolina Copacking, LLC initiated this food recall on December 13, 2023. The FDA enforcement report states: During a contract inspection by the North Carolina Department of Agriculture, NCDA, informed the firm that the labeling does not list the common name of "milk". The FDA report lists distribution as: Product was shipped to one customer in VA.

The FDA enforcement report describes the reason as: During a contract inspection by the North Carolina Department of Agriculture, NCDA, informed the firm that the labeling does not list the common name of "milk".

Scratch Pasta Co Marinara Sauce NET WT was made or distributed by Carolina Copacking, LLC in Henderson, NC, United States. This page reflects FDA report F-0688-2024, dated January 10, 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, 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 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 Scratch Pasta Co Marinara Sauce NET WT recall?

Carolina Copacking, LLC recalled Scratch Pasta Co Marinara Sauce NET WT in an FDA Class II enforcement action reported as F-0688-2024. During a contract inspection by the North Carolina Department of Agriculture, NCDA, informed the firm that the labeling does not list the common name of "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 Carolina Copacking, 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-0688-2024 and keep the packaging, lot code and proof of purchase if you have them.

Is the Carolina Copacking, LLC recall still active?

Yes. As of the latest FDA enforcement report, this recall is listed as ongoing. Check the official source record for the most current status before making a decision.

Where can I verify this recall?

This page is normalized from the openFDA enforcement record F-0688-2024. 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

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