CLASS I ONGOING Food recall · Reported 10 Jun 2026 · FDA Enforcement Report

Hellas Meze Golden Smoked Whole Herring recalled by Terra Medi

Terra Medi is recalling Hellas Meze Golden Smoked Whole Herring, distributed in Illinois, Massachusetts, New Jersey, New York. The recall was initiated on 13 May 2026 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesproduction date of 4/12/2025, best before 4/12/2026, L120425F54
Quantity recalled20 cases (15 units per case)

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-0899-2026
FDA event ID
98989
Recalling firm
Terra Medi, Long Island City, NY
Classification
Class I
Status
Ongoing
Recall initiated
13 May 2026
FDA classified
2 Jun 2026
Reported
10 Jun 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

13 May 2026Recall initiated by company
2 Jun 2026Classified by FDA+20 days
10 Jun 2026Published in enforcement report+8 days

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

Reason for recall

Un-eviscerated fish may be contaminated with clostridium botulinum

Product as listed by the FDA

Hellas Meze Golden Smoked Whole Herring

Where it was distributed

MA, NJ, IL, and NY

IllinoisMassachusettsNew JerseyNew York

Questions about this recall

Why was it recalled?

Un-eviscerated fish may be contaminated with clostridium botulinum

Which lots are affected?

production date of 4/12/2025, best before 4/12/2026, L120425F54

Where was it sold?

MA, NJ, IL, and NY

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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