Toshoku

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

Refusal charges, in plain English

• UNSAFE COL2 refused lines

  Color additive unsafe under section 721

  The product appeared to be, or to contain, a color additive that is unsafe within the meaning of section 721(a) of the FD&C Act, the section that governs which color additives may be used and how.

• COLOR LBLG1 refused line

  Artificial coloring not declared

  The product appeared to contain an artificial coloring without labeling that states that fact.

• 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 Toshoku

Is Toshoku on an FDA import alert?

Yes. As of October 25, 2026, Toshoku is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for sours gummy "chibi sours drink assort gumi"; FDA published the listing on November 8, 2018.

Has FDA refused shipments from Toshoku?

Yes. FDA refused 3 shipment lines from Toshoku between November 1, 2018 and May 3, 2019. The most recent, on May 3, 2019, was beverage base not mentioned elsewhere, n.e.c., charged as NEEDS FCE (processor not registered for canned or acidified foods).

Why did FDA refuse Toshoku's shipments?

The most frequent charges are UNSAFE COL (color additive unsafe under section 721, 2 lines) and COLOR LBLG (artificial coloring not declared, 1 line).

What is Toshoku's FEI number?

Toshoku's FDA Establishment Identifier (FEI) is 3010229406.

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

Shipments of sours gummy "chibi sours drink assort gumi" from Toshoku can be detained without physical examination under Import Alert 45-02; 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).