Has FDA refused shipments from Onoguchi Co., Ltd.?

Yes. FDA refused 4 shipment lines from Onoguchi Co., Ltd. between May 20, 2020 and July 30, 2021. The most recent, on July 30, 2021, was gourd, dried or paste, charged as SULFITELBL (sulfitelbl).

Why did FDA refuse Onoguchi Co., Ltd.'s shipments?

The most frequent charges are SULFITELBL (sulfitelbl, 4 lines) and LIST INGRE (ingredients not listed, 1 line).

What is Onoguchi Co., Ltd.'s FEI number?

Onoguchi Co., Ltd.'s FDA Establishment Identifier (FEI) is 1000194871.

Can shipments from Onoguchi Co., Ltd. still enter the U.S.?

Shipments of gourd, dried or paste from Onoguchi Co., Ltd. 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).

Onoguchi Co., Ltd.

FDA import alert and refusal historyTochigi, JapanFEI 1000194871

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As of October 25, 2026, Onoguchi Co., Ltd. (Tochigi, 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 4 FDA import refusals recorded since October 2016.

Data from FDA public records, last checked October 25, 2026. Request a correction

Current status

Import alerts: IA 99-21 · red list
Last import refusal: Jul 30, 2021Gourd, dried or paste · SULFITELBL
Last warning letter: None found
Last inspection: None on record

Every FDA record for Onoguchi Co., Ltd.

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

2021

Jul 30, 2021Import refusal
Refused, Gourd, dried or pasteSULFITELBL LIST INGREEntry 235-1661982-4
Source

2020

Dec 1, 2020Import refusal
Refused, Gourd, dried or pasteSULFITELBLEntry 235-1649027-5
Source
Nov 18, 2020Import refusal
Refused, Gourd, dried or pasteSULFITELBLEntry 235-1648081-3
Source
May 20, 2020Import refusal
Refused, Gourd, dried or pasteSULFITELBLEntry 235-1639830-4
Source

2009

Sep 16, 2009Import alert listing
Listed on Import Alert 99-21red listGourd, Dried or Paste
Source

Refusal charges, in plain English

SULFITELBL4 refused lines
SULFITELBL
LIST INGRE1 refused line
Ingredients not listed
The product is made from two or more ingredients and the label appeared not to list the common or usual name of each one (or, for a juice beverage, the percentage of juice).

Questions about Onoguchi Co., Ltd.

Is Onoguchi Co., Ltd. on an FDA import alert?: Yes. As of October 25, 2026, Onoguchi Co., Ltd. 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 Onoguchi Co., Ltd.?: Yes. FDA refused 4 shipment lines from Onoguchi Co., Ltd. between May 20, 2020 and July 30, 2021. The most recent, on July 30, 2021, was gourd, dried or paste, charged as SULFITELBL (sulfitelbl).
Why did FDA refuse Onoguchi Co., Ltd.'s shipments?: The most frequent charges are SULFITELBL (sulfitelbl, 4 lines) and LIST INGRE (ingredients not listed, 1 line).
What is Onoguchi Co., Ltd.'s FEI number?: Onoguchi Co., Ltd.'s FDA Establishment Identifier (FEI) is 1000194871.
Can shipments from Onoguchi Co., Ltd. still enter the U.S.?: Shipments of gourd, dried or paste from Onoguchi Co., Ltd. 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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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.