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
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
- Brand
- MA Cohen's
- 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 2026 | Recall initiated by company | |
| 20 May 2026 | Classified by FDA | +22 days |
| 27 May 2026 | Published 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
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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