EBADA FISHERY Co.,Ltd
FDA import alert and refusal historySeo-gu, South KoreaFEI 3013782384
As of October 26, 2026, EBADA FISHERY Co.,Ltd (Seo-gu, South Korea) is on the red list of FDA Import Alert 16-39 (Ready-to-eat seafood: Listeria monocytogenes) for stir fried eel (hagfish), published by FDA on November 26, 2019, and has 3 FDA import refusals recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 16-39 · red list
- Last import refusal
- Eel · LISTERIA
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for EBADA FISHERY Co.,Ltd
4 records, newest first. Each line links to the FDA page it came from.
Refusal charges, in plain English
- LISTERIA3 refused lines
Listeria monocytogenes
The product appeared to contain Listeria monocytogenes, which the law treats as a poisonous and deleterious substance that may make food injurious to health.
Questions about EBADA FISHERY Co.,Ltd
- Is EBADA FISHERY Co.,Ltd on an FDA import alert?
- Yes. As of October 26, 2026, EBADA FISHERY Co.,Ltd is on the red list of FDA Import Alert 16-39, “Ready-to-eat seafood: Listeria monocytogenes”, for stir fried eel (hagfish); FDA published the listing on November 26, 2019.
- Has FDA refused shipments from EBADA FISHERY Co.,Ltd?
- Yes. FDA refused 3 shipment lines from EBADA FISHERY Co.,Ltd between December 11, 2019 and May 20, 2020. The most recent, on May 20, 2020, was eel, charged as LISTERIA (listeria monocytogenes).
- Why did FDA refuse EBADA FISHERY Co.,Ltd's shipments?
- The most frequent charge is LISTERIA (listeria monocytogenes, 3 lines).
- What is EBADA FISHERY Co.,Ltd's FEI number?
- EBADA FISHERY Co.,Ltd's FDA Establishment Identifier (FEI) is 3013782384.
- Can shipments from EBADA FISHERY Co.,Ltd still enter the U.S.?
- Shipments of stir fried eel (hagfish) from EBADA FISHERY Co.,Ltd can be detained without physical examination under Import Alert 16-39; FDA releases them only if evidence shows they do not have the listed violation. Importers must consider this listing in their FSVP evaluation (21 CFR 1.505).
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SupplierRadar is not affiliated with the U.S. Food and Drug Administration. Data comes from public FDA records and may contain errors. This is not legal advice; importers remain responsible for their supplier evaluations.