Has FDA refused shipments from Kinokomura?

Yes. FDA refused 3 shipment lines from Kinokomura between May 17, 2022 and May 19, 2023. The most recent, on May 19, 2023, was enokitake, charged as LISTERIA (listeria monocytogenes).

Why did FDA refuse Kinokomura's shipments?

The most frequent charge is LISTERIA (listeria monocytogenes, 3 lines).

What is Kinokomura's FEI number?

Kinokomura's FDA Establishment Identifier (FEI) is 3014336506.

Can shipments from Kinokomura still enter the U.S.?

Shipments of amashaki aji-enoki (enokitake mushroom) from Kinokomura can be detained without physical examination under Import Alert 99-23; 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).

Kinokomura

FDA import alert and refusal historySuzaka, JapanFEI 3014336506

Recorded by FDA as KINOKOMURA

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As of October 27, 2026, Kinokomura (Suzaka, Japan) is on the red list of FDA Import Alert 99-23 (Produce: contamination with human pathogens) for amashaki aji-enoki (enokitake mushroom), published by FDA on July 12, 2022, and has 3 FDA import refusals recorded since October 2016.

Data from FDA public records, last checked October 27, 2026. Request a correction

Current status

Import alerts: IA 99-23 · red list
Last import refusal: May 19, 2023Enokitake · LISTERIA
Last warning letter: None found
Last inspection: None on record

Every FDA record for Kinokomura

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

2023

May 19, 2023Import refusal
Refused, 2 lines in one entry: EnokitakeLISTERIAEntry 235-1700138-6Show 2 linesHide lines
- Refused, EnokitakeLISTERIAEntry 235-1700138-6Source
- Refused, EnokitakeLISTERIAEntry 235-1700138-6Source
Source

2022

Jul 12, 2022Import alert listing
Listed on Import Alert 99-23red listAmashaki aji-enoki (enokitake mushroom)
Source
May 17, 2022Import refusal
Refused, Enokitake mushrooms, whole (button) (fungi)LISTERIAEntry 597-0200410-8
Source

Refusal charges, in plain English

LISTERIA3 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 Kinokomura

Is Kinokomura on an FDA import alert?: Yes. As of October 27, 2026, Kinokomura is on the red list of FDA Import Alert 99-23, “Produce: contamination with human pathogens”, for amashaki aji-enoki (enokitake mushroom); FDA published the listing on July 12, 2022.
Has FDA refused shipments from Kinokomura?: Yes. FDA refused 3 shipment lines from Kinokomura between May 17, 2022 and May 19, 2023. The most recent, on May 19, 2023, was enokitake, charged as LISTERIA (listeria monocytogenes).
Why did FDA refuse Kinokomura's shipments?: The most frequent charge is LISTERIA (listeria monocytogenes, 3 lines).
What is Kinokomura's FEI number?: Kinokomura's FDA Establishment Identifier (FEI) is 3014336506.
Can shipments from Kinokomura still enter the U.S.?: Shipments of amashaki aji-enoki (enokitake mushroom) from Kinokomura can be detained without physical examination under Import Alert 99-23; 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.