CLASS III ONGOING Food recall · Reported 17 Dec 2025 · FDA Enforcement Report

Shloimy's Heimishe Matjes Herring recalled by Kosher First

Kosher First is recalling Shloimy's Heimishe Matjes Herring, distributed in New York. The recall was initiated on 10 Nov 2025 and the FDA has classified it as Class III.

Check your package

Lot, batch or date codesBatch Code: 0103
Quantity recalled283 units

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
H-0238-2026
FDA event ID
98005
Recalling firm
Kosher First, Brooklyn, NY
Classification
Class III
Status
Ongoing
Recall initiated
10 Nov 2025
FDA classified
5 Dec 2025
Reported
17 Dec 2025
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Undeclared Allergens
Product category
Other

Timeline

10 Nov 2025Recall initiated by company
5 Dec 2025Classified by FDA+25 days
17 Dec 2025Published in enforcement report+12 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Undeclared FD&C Red #40

Food allergen labelling is required by US law for the nine major allergens. A product recalled for an undeclared allergen is only a risk to people with that allergy; everyone else can consume it safely.

Product as listed by the FDA

Shloimy's Heimishe Matjes Herring packaged in 7oz plastic container

Where it was distributed

New York

New York

Questions about this recall

Is Shloimy's Heimishe Matjes Herring recalled?

Yes. Kosher First recalled Shloimy's Heimishe Matjes Herring on 10 Nov 2025. The recall is Class III and its status is Ongoing. Recall number H-0238-2026.

Why was it recalled?

Undeclared FD&C Red #40

Which lots are affected?

Batch Code: 0103

Where was it sold?

New York

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class III mean?

Class III recalls are for products unlikely to cause any adverse health consequence, usually labelling or quality issues.

Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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