Fresh Recalls

FDAClass II · Food · Recall H-1198-2026 · Recalled August 12, 2026

FLOUNDER SASHIMI WITH SAUCE recall — Eunha Fisheries Co., LTD

Agency report date: August 12, 2026.

1. Compare your item

This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.

Product named
FLOUNDER SASHIMI WITH SAUCE
Company / brand
Eunha Fisheries Co
Lot / serial / date codes
Best By date: 2026.07.11; 2026.12.08
Distribution
CA, NJ
Agency product description and boundaries

FLOUNDER SASHIMI WITH SAUCE; Keep Frozen; Net WT: 300g; UPC: 8 809342 366186

Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.

If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.

2. Agency hazard and consumer action

FDA reports: Foreign Manufacturer label contains Undeclared allergen ingredients Wheat, Soy, Sesame, Yellow #5 and Blue #1 in Frozen Flounder Products.

No consumer remedy instructions are supplied in this record. Check the official notice and listed company contact for the agency’s current instructions.

Class II: may cause temporary or medically reversible health consequences.

Affected product: FLOUNDER SASHIMI WITH SAUCE

3. Open the official notice or contact

Official recall ID
H-1198-2026
Brand
Eunha Fisheries Co
Classification
Class II
Units affected
445 units
Recall status
Ongoing
Initiated
Voluntary: Firm initiated

Affected products

Companies & origin

Recalling firm location
Gangseo, Korea (the Republic of)
Firm address
36 Noksansandan 381-Ro, N/A

Identifying details (verbatim from the notice)

Product codes / lots
Best By date: 2026.07.11; 2026.12.08
Distribution
CA, NJ
Firm notified the public via
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
FDA event ID
99351
Recall initiated
July 1, 2026
FDA classified
August 4, 2026
FDA report date
August 12, 2026
Verify with the official sources:

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Source: U.S. Food & Drug Administration. Agency excerpts come from the public data feed and may omit tables or later changes; the linked government source is authoritative. Source last checked September 7, 2026 at 6:00 AM UTC. Record retrieved September 7, 2026 at 6:00 AM UTC.

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