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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Food
Food & Beverages/Dairy & Eggs

Kabobs Brie En Croute with Raspberry Recalled for Listeria Risk

Agency Publication Date: October 31, 2022
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Summary

Kabobs Acquisition Inc. is recalling 25 cases of Brie En Croute with Raspberry because the brie cheese supplier notified the firm of potential contamination with Listeria monocytogenes. The recall affects Product K7135 with Lot # PM22J07. Consumers who have this product should not eat it and should return it to the place of purchase for a full refund or dispose of it immediately.

Risk

The product may be contaminated with Listeria monocytogenes, an organism that can cause serious and sometimes fatal infections in young children, elderly people, and those with weakened immune systems. Although healthy individuals may only suffer short-term symptoms like high fever, severe headache, and nausea, Listeria infection can cause miscarriages and stillbirths among pregnant women.

What You Should Do

  1. This recall involves Kabobs Brie En Croute with Raspberry, identified as Product K7135 with Lot # PM22J07.
  2. Return the product to the place of purchase for a refund, throw it away, or contact Kabobs Acquisition Inc. for further instructions.
  3. Call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) for additional questions.

Your Remedy Options

You have 2 options:

๐Ÿ’ฐOption 1: Full Refund
How to: Return the product to the place of purchase for a full refund, or contact the manufacturer or supplier for further instructions
๐Ÿ—‘๏ธOption 2: Dispose of Product
How to: Throw the product away.

Affected Products

Product: Brie En Croute with Raspberry
Item Code:
K7135
Lot Numbers:
PM22J07

Recall #: F-0081-2023; Product was shipped to one distributor in Georgia.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 90951
Status: Active
Manufacturer: Kabobs Acquisition Inc.
Sold By: One distributor in Georgia
Manufactured In: United States
Units Affected: 25 cases
Distributed To: Georgia

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.