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Kasakurashigeyoshi Shoten

FDA import alert and refusal historyKawachi, JapanFEI 1000134203

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Example subjectKasakurashigeyoshi Shote added to Import Alert 16-129 (red list)

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As of October 26, 2026, Kasakurashigeyoshi Shoten (Kawachi, Japan) is on the red list of FDA Import Alert 99-21 (Foods with undeclared added sulfiting agents) for gourd, dried or paste, published by FDA on September 16, 2009, 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 Kasakurashigeyoshi Shoten

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

2009

  1. Import alert listing
    Listed on Import Alert 99-21red listGourd, Dried or Paste
    Source

Questions about Kasakurashigeyoshi Shoten

Is Kasakurashigeyoshi Shoten on an FDA import alert?
Yes. As of October 26, 2026, Kasakurashigeyoshi Shoten is on the red list of FDA Import Alert 99-21, “Foods with undeclared added sulfiting agents”, for gourd, dried or paste; FDA published the listing on September 16, 2009.
Has FDA refused shipments from Kasakurashigeyoshi Shoten?
No FDA import refusals for Kasakurashigeyoshi Shoten appear in FDA's refusal data since October 2016, as of October 26, 2026.
What is Kasakurashigeyoshi Shoten's FEI number?
Kasakurashigeyoshi Shoten's FDA Establishment Identifier (FEI) is 1000134203.
Can shipments from Kasakurashigeyoshi Shoten still enter the U.S.?
Shipments of gourd, dried or paste from Kasakurashigeyoshi Shoten can be detained without physical examination under Import Alert 99-21; 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 subjectKasakurashigeyoshi Shote 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.