Mametaro Co.,LTD

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

Refusal charges, in plain English

• COLOR LBLG1 refused line

  Artificial coloring not declared

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

• UNSAFE COL1 refused line

  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.

Questions about Mametaro Co.,LTD

Is Mametaro Co.,LTD on an FDA import alert?

No listing for Mametaro Co.,LTD appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Japan page.

Has FDA refused shipments from Mametaro Co.,LTD?

Yes. FDA refused 2 shipment lines from Mametaro Co.,LTD between June 3, 2023 and August 22, 2025. The most recent, on August 22, 2025, was ginger root (root & tuber vegetable), charged as UNSAFE COL (color additive unsafe under section 721).

Why did FDA refuse Mametaro Co.,LTD's shipments?

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

What is Mametaro Co.,LTD's FEI number?

Mametaro Co.,LTD's FDA Establishment Identifier (FEI) is 3017203008.