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AJIRUSHI CO., LTD. - Main Plant

FDA import alert and refusal historyHitachinaka, JapanFEI 1000258142

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Example subjectAJIRUSHI CO., LTD. - Main Plan added to Import Alert 16-129 (red list)

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As of October 26, 2026, AJIRUSHI CO., LTD. - Main Plant (Hitachinaka, Japan) is on the red list of FDA Import Alert 16-39 (Ready-to-eat seafood: Listeria monocytogenes) for seasoned cuttlefish; octopus, published by FDA on May 15, 2013, 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 16-39 · red list
Last import refusal
Octopus, other aquatic species · LISTERIA
Last warning letter
None found
Last inspection
None on record

Every FDA record for AJIRUSHI CO., LTD. - Main Plant

3 records, newest first. Each line links to the FDA page it came from.

2024

  1. Import refusal
    Refused, 2 lines in one entry: Octopus, other aquatic speciesLISTERIAEntry EH3-2473943-0Show 2 lines
    Source

2013

  1. Import alert listing
    Listed on Import Alert 16-39red listSeasoned Cuttlefish; Octopus
    Source

Refusal charges, in plain English

  • LISTERIA2 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 AJIRUSHI CO., LTD. - Main Plant

Is AJIRUSHI CO., LTD. - Main Plant on an FDA import alert?
Yes. As of October 26, 2026, AJIRUSHI CO., LTD. - Main Plant is on the red list of FDA Import Alert 16-39, “Ready-to-eat seafood: Listeria monocytogenes”, for seasoned cuttlefish; octopus; FDA published the listing on May 15, 2013.
Has FDA refused shipments from AJIRUSHI CO., LTD. - Main Plant?
Yes. FDA refused 2 shipment lines from AJIRUSHI CO., LTD. - Main Plant on August 2, 2024. The most recent, on August 2, 2024, was octopus, other aquatic species, charged as LISTERIA (listeria monocytogenes).
Why did FDA refuse AJIRUSHI CO., LTD. - Main Plant's shipments?
The most frequent charge is LISTERIA (listeria monocytogenes, 2 lines).
What is AJIRUSHI CO., LTD. - Main Plant's FEI number?
AJIRUSHI CO., LTD. - Main Plant's FDA Establishment Identifier (FEI) is 1000258142.
Can shipments from AJIRUSHI CO., LTD. - Main Plant still enter the U.S.?
Shipments of seasoned cuttlefish; octopus from AJIRUSHI CO., LTD. - Main Plant 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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Example subjectAJIRUSHI CO., LTD. - Main Plan added to Import Alert 16-129 (red list)

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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.