Itoh trading Co.,Ltd.
FDA import alert and refusal historyMizunami City, JapanFEI 3004253967
As of October 25, 2026, Itoh trading Co.,Ltd. (Mizunami City, Japan) is on the red list of FDA Import Alert 16-81 (Seafood products: Salmonella) for dried scallops, published by FDA on September 18, 2009, and has 1 FDA import refusal 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
- Scallops · SALMONELLA
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Itoh trading Co.,Ltd.
2 records, newest first. Each line links to the FDA page it came from.
2023
- Import refusalRefused, ScallopsSALMONELLAEntry KL1-0274998-5Source
2009
- Import alert listingListed on Import Alert 16-81red listDried ScallopsSource
Refusal charges, in plain English
- SALMONELLA1 refused line
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 Itoh trading Co.,Ltd.
- Is Itoh trading Co.,Ltd. on an FDA import alert?
- Yes. As of October 25, 2026, Itoh trading Co.,Ltd. is on the red list of FDA Import Alert 16-81, “Seafood products: Salmonella”, for dried scallops; FDA published the listing on September 18, 2009.
- Has FDA refused shipments from Itoh trading Co.,Ltd.?
- Yes. FDA refused 1 shipment line from Itoh trading Co.,Ltd. on December 1, 2023. The most recent, on December 1, 2023, was scallops, charged as SALMONELLA (salmonella).
- Why did FDA refuse Itoh trading Co.,Ltd.'s shipments?
- The most frequent charge is SALMONELLA (salmonella, 1 line).
- What is Itoh trading Co.,Ltd.'s FEI number?
- Itoh trading Co.,Ltd.'s FDA Establishment Identifier (FEI) is 3004253967.
- Can shipments from Itoh trading Co.,Ltd. still enter the U.S.?
- Shipments of dried scallops from Itoh trading Co.,Ltd. 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.