RecallHawk
Class I Recall

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

Shining Sea Fish Co. LLC

Summary

The FDA issued a Class I for MA Cohen's Kippered Herring vacuum packed, weight provided at retail, UPC 72325 by Shining Sea Fish Co. LLC. Reason: Clostridium botulinum is an uncontrolled hazard.

Details

Source

Food Recall

External ID

H-0810-2026

Action Date

2026-05-27

Status

Terminated

Category

food

Product Description

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

Lot/Code Info: LOT 25079 Expiration May 03 2026, LOT 25055 Expiration May 12 2026, LOT 25028 Expiration June 03 2026, LOT 26344 Expiration July 22 2026

Quantity Affected: 675 pounds

Reason for Recall

Clostridium botulinum is an uncontrolled hazard

Distribution

MI

Type: Voluntary: Firm initiated

Recall Initiated: 2026-04-28

Company

Context & Analysis

This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.

This was one of 80 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Frequently Asked Questions

What is a Class I recall?

A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Shining Sea Fish Co. LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Shining Sea Fish Co. LLC have FDA actions?

This is the only FDA action we have on record for Shining Sea Fish Co. LLC in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "H-0810-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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