Kuroda Shokuhin

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

Refusal charges, in plain English

• UNSAFE ADD2 refused lines

  Food additive unsafe under section 409

  The product appeared to contain a food additive that is unsafe within the meaning of section 409 of the FD&C Act, the section that governs which food additives may be used and under what conditions.

• NEEDS FCE1 refused line

  Processor not registered for canned or acidified foods

  The manufacturer appeared not to be registered with FDA as a low-acid canned food or acidified food processor, as 21 CFR 108.25 and 108.35 require.

• NO PROCESS1 refused line

  No scheduled process filed

  The manufacturer appeared not to have filed a scheduled process with FDA, which 21 CFR Part 108 requires for low-acid canned and acidified foods, so the product is treated as made under insanitary conditions.

Questions about Kuroda Shokuhin

Is Kuroda Shokuhin on an FDA import alert?

Yes. As of October 26, 2026, Kuroda Shokuhin is on the red list of FDA Import Alert 45-06, “Stevia leaves, crude extracts and foods containing them”, for pickled radish; FDA published the listing on August 11, 2010.

Has FDA refused shipments from Kuroda Shokuhin?

Yes. FDA refused 3 shipment lines from Kuroda Shokuhin between September 12, 2017 and July 20, 2018. The most recent, on July 20, 2018, was chinese radish (daikon) (root & tuber vegetable), charged as UNSAFE ADD (food additive unsafe under section 409).

Why did FDA refuse Kuroda Shokuhin's shipments?

The most frequent charges are UNSAFE ADD (food additive unsafe under section 409, 2 lines) and NEEDS FCE (processor not registered for canned or acidified foods, 1 line).

What is Kuroda Shokuhin's FEI number?

Kuroda Shokuhin's FDA Establishment Identifier (FEI) is 3004299309.

Can shipments from Kuroda Shokuhin still enter the U.S.?

Shipments of pickled radish from Kuroda Shokuhin can be detained without physical examination under Import Alert 45-06; 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).