CLASS I Food recall · Reported 27 May 2026 · FDA Enforcement Report

MA Cohen's Kippered Herring vacuum packed, weight provided at retail recalled

Shining Sea Fish Co is recalling MA Cohen's Kippered Herring vacuum packed, weight provided at retail, distributed in Michigan. The recall was initiated on 28 Apr 2026 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesLOT 25079 Expiration May 03 2026, LOT 25055 Expiration May 12 2026, LOT 25028 Expiration June 03 2026, LOT 26344 Expiration July 22 2026
Quantity recalled675 pounds

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-0810-2026
FDA event ID
98886
Recalling firm
Shining Sea Fish Co, Detroit, MI
Classification
Class I
Status
Terminated
Recall initiated
28 Apr 2026
FDA classified
20 May 2026
Reported
27 May 2026
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Botulism
Product category
Other

Timeline

28 Apr 2026Recall initiated by company
20 May 2026Classified by FDA+22 days
27 May 2026Published in enforcement report+7 days

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

Reason for recall

Clostridium botulinum is an uncontrolled hazard

Product as listed by the FDA

MA Cohen's Kippered Herring vacuum packed, weight provided at retail, UPC 7232577992

Where it was distributed

MI

Michigan

Questions about this recall

Why was it recalled?

Clostridium botulinum is an uncontrolled hazard

Which lots are affected?

LOT 25079 Expiration May 03 2026, LOT 25055 Expiration May 12 2026, LOT 25028 Expiration June 03 2026, LOT 26344 Expiration July 22 2026

Where was it sold?

MI

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 I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 26 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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