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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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Low RiskFDA Food
Food & Beverages/Packaged & Processed

Shloimy's Heimishe Matjes Herring Recalled for Undeclared FD&C Red #40

Agency Publication Date: December 5, 2025
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Summary

Kosher First LLC is recalling approximately 283 units of Shloimy's Heimishe Matjes Herring because the product contains the food coloring FD&C Red #40, which is not declared on the label. The recalled herring was sold in 7oz plastic containers in New York. Consumers should return the product to the place of purchase for a full refund or contact the manufacturer for more information.

Risk

People who have an allergy or sensitivity to FD&C Red #40 may experience an allergic reaction if they consume this product.

What You Should Do

  1. Check your container for Shloimy's Heimishe Matjes Herring in a 7oz plastic size with Batch Code 0103.
  2. Return the product to the place of purchase for a full refund, throw it away, or contact Kosher First LLC 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: Shloimy's Heimishe Matjes Herring (7oz)
Item Code:
H-0238-2026
Lot Numbers:
Batch Code: 0103

Packaged in plastic container

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 98005
Status: Active
Manufacturer: Kosher First LLC
Manufactured In: United States
Units Affected: 283 units
Distributed To: New York

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.