Ika
FDA import alert and refusal historyPusan, South KoreaFEI 3011119660
Recorded by FDA as IKA
As of October 26, 2026, Ika (Pusan, South Korea) is on the red list of FDA Import Alert 16-81 (Seafood products: Salmonella) for filefish "seasoned filefish", published by FDA on January 5, 2021, and has 2 FDA import refusals recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 16-81 · red list
- Last import refusal
- Filefish, hot smoked, fish · SALMONELLA
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Ika
3 records, newest first. Each line links to the FDA page it came from.
2021
- Import refusalSource
Refused, 2 lines in one entry: Filefish, hot smoked, fishSALMONELLAEntry E7T-0929205-0Show 2 linesHide lines
- Refused, Filefish, hot smoked, fishSALMONELLAEntry E7T-0929205-0Source
- Refused, Filefish, hot smoked, fishSALMONELLAEntry E7T-0929205-0Source
- Import alert listingListed on Import Alert 16-81red listFilefish "Seasoned Filefish"Source
Refusal charges, in plain English
- SALMONELLA2 refused lines
Salmonella
The product appeared to contain Salmonella, which the law treats as a poisonous and deleterious substance that may make food injurious to health.
Questions about Ika
- Is Ika on an FDA import alert?
- Yes. As of October 26, 2026, Ika is on the red list of FDA Import Alert 16-81, “Seafood products: Salmonella”, for filefish "seasoned filefish"; FDA published the listing on January 5, 2021.
- Has FDA refused shipments from Ika?
- Yes. FDA refused 2 shipment lines from Ika on January 25, 2021. The most recent, on January 25, 2021, was filefish, hot smoked, fish, charged as SALMONELLA (salmonella).
- Why did FDA refuse Ika's shipments?
- The most frequent charge is SALMONELLA (salmonella, 2 lines).
- What is Ika's FEI number?
- Ika's FDA Establishment Identifier (FEI) is 3011119660.
- Can shipments from Ika still enter the U.S.?
- Shipments of filefish "seasoned filefish" from Ika can be detained without physical examination under Import Alert 16-81; 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.