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Daikatsu Suisan Co., Ltd.

FDA import alert and refusal historyHigashi Ibaraki-Gun, Ibaraki, JapanFEI 3004134912

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Example subjectDaikatsu Suisan Co., Ltd added to Import Alert 16-129 (red list)

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As of October 26, 2026, Daikatsu Suisan Co., Ltd. (Higashi Ibaraki-Gun, Ibaraki, Japan) is on the red list of FDA Import Alert 16-39 (Ready-to-eat seafood: Listeria monocytogenes) for prepared mackerel, published by FDA on November 24, 2010, and has no FDA import refusals recorded since October 2016.

Data from FDA public records, last checked . Request a correction

Current status

Last import refusal
None since October 2016
Last warning letter
None found
Last inspection
None on record

Every FDA record for Daikatsu Suisan Co., Ltd.

1 record, newest first. Each line links to the FDA page it came from.

2010

  1. Import alert listing
    Listed on Import Alert 16-39red listPrepared Mackerel
    Source

Questions about Daikatsu Suisan Co., Ltd.

Is Daikatsu Suisan Co., Ltd. on an FDA import alert?
Yes. As of October 26, 2026, Daikatsu Suisan Co., Ltd. is on the red list of FDA Import Alert 16-39, “Ready-to-eat seafood: Listeria monocytogenes”, for prepared mackerel; FDA published the listing on November 24, 2010.
Has FDA refused shipments from Daikatsu Suisan Co., Ltd.?
No FDA import refusals for Daikatsu Suisan Co., Ltd. appear in FDA's refusal data since October 2016, as of October 26, 2026.
What is Daikatsu Suisan Co., Ltd.'s FEI number?
Daikatsu Suisan Co., Ltd.'s FDA Establishment Identifier (FEI) is 3004134912.
Can shipments from Daikatsu Suisan Co., Ltd. still enter the U.S.?
Shipments of prepared mackerel from Daikatsu Suisan 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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Example subjectDaikatsu Suisan Co., Ltd 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.