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Lower risk Food recall · FDA · Published November 10, 2025

Shloimy's Heimishe Matjes Herring Recall: Undeclared Red #40 Food Dye

Kosher First LLC recalls Shloimy's Heimishe Matjes Herring in 7oz plastic containers due to undeclared FD&C Red #40. Consumers should check batch code 0103 for affected products.

🇺🇸 FDA recall #H-0238-2026FoodShloimy's Heimis: Kosher First LLC ›
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Contact the company

Recalling firmKosher First LLC502 Flushing Ave · Brooklyn, NY 11205-1616
✎ GovInfoNow plain-language explainer

Kosher First LLC is recalling Shloimy's Heimishe Matjes Herring in 7oz plastic containers because they contain undeclared FD&C Red #40 food dye. This could pose a risk for people with food allergies or sensitivities to this dye. Read more at govinfonow.com/recall/6989-shloimy-s-heimishe-matjes-herring-recall-undeclared-red-40-food.

Source Summary by GovInfoNow · govinfonow.com/recall/6989-shloimy-s-heimishe-matjes-herring-recall-undeclared-red-40-food · Updated August 17, 2026 · Official notice: FDA #H-0238-2026

Cite this page

“Shloimy's Heimishe Matjes Herring Recall: Undeclared Red #40 Food Dye.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/6989-shloimy-s-heimishe-matjes-herring-recall-undeclared-red-40-food. Based on FDA recall #H-0238-2026.

The FDA announced on Nov. 10, 2025, that Kosher First LLC voluntarily recalled Shloimy's Heimishe Matjes Herring due to undeclared FD&C Red #40. The recall affects 283 units distributed in New York.

How to tell if you have it

  • Brand: Shloimy's Heimis
  • Product: Shloimy's Heimishe Matjes Herring packaged in 7oz plastic container
  • Batch Code: 0103

The hazard

The product contains undeclared FD&C Red #40, an allergen that may pose a risk to consumers with sensitivities.

Context

GovInfoNow's records show other recent recalls of similar products include Bombay Kitchen Tikka Sev Recall (2026-03-25) and Bombay Kitchen Punjabi Mix Recall (2026-03-25), both citing undeclared colors. Wonton Specialists Wonton Skin Recall (2026-07-28) also cited undeclared Red 40 food dye.

How to tell if you have this one

Check for Shloimy's Heimishe Matjes Herring in 7oz plastic containers with batch code 0103. The product is sold by Kosher First LLC.

  • Brand
    Shloimy's Heimis: Kosher First LLC
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Product Label

    Look for the batch code 0103 on the container to confirm if it's affected.

Where it went and when

Where it was distributed

Distributed in New York.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: not listedILWisconsin: not listedWIMichigan: not listedMINew York: yesNYRhode Island: not listedRIMassachusetts: not listedMAOregon: not listedORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: not listedOHPennsylvania: not listedPANew Jersey: not listedNJConnecticut: not listedCTCalifornia: not listedCAUtah: not listedUTColorado: not listedCONebraska: not listedNEMissouri: not listedMOKentucky: not listedKYWest Virginia: not listedWVVirginia: not listedVAMaryland: not listedMDDelaware: not listedDEArizona: not listedAZNew Mexico: not listedNMKansas: not listedKSArkansas: not listedARTennessee: not listedTNNorth Carolina: not listedNCSouth Carolina: not listedSCDistrict of Columbia: not listedDCOklahoma: not listedOKLouisiana: not listedLAMississippi: not listedMSAlabama: not listedALGeorgia: not listedGAHawaii: not listedHITexas: not listedTXFlorida: not listedFL

FDA distribution: “New York” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: New York.

Recall timeline

FDA published this recall 37 days after the firm started it.

1. Firm started the recall: Nov 10, 202512. FDA classified it Class III: Dec 5, 202523. Published in FDA’s Enforcement Report: Dec 17, 202532025
  1. Firm started the recall
  2. FDA classified it Class III
  3. Published in FDA’s Enforcement Report

Dates from the agency record only; steps without a date are left out.

✎ GovInfoNow

Questions people ask

What should I do if I have the recalled product?

The recall does not include a specific remedy, so you should check the product label for the batch code and avoid it if you have a sensitivity to FD&C Red #40.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #H-0238-2026 (November 10, 2025)
  • Plain-language summary written by qwen3:4b on August 17, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA