Is Eishindo on an FDA import alert?

No listing for Eishindo appears in the FDA import alerts SupplierRadar checked on October 25, 2026. Country-wide alerts may still apply to its products; see the Japan page.

Has FDA refused shipments from Eishindo?

Yes. FDA refused 3 shipment lines from Eishindo between February 9, 2021 and April 2, 2021. The most recent, on April 2, 2021, was gel cups, fruit flavored, charged as UNSAFE COL (color additive unsafe under section 721).

Why did FDA refuse Eishindo's shipments?

The most frequent charges are FOREIGN OB (foreign ob, 2 lines) and UNSAFE COL (color additive unsafe under section 721, 2 lines).

What is Eishindo's FEI number?

Eishindo's FDA Establishment Identifier (FEI) is 3010124844.

Eishindo

FDA import alert and refusal historyAmagasaki, JapanFEI 3010124844

Recorded by FDA as EISHINDO

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As of October 25, 2026, Eishindo is not on any FDA import alert in SupplierRadar's records; FDA refused 3 of its shipment lines between February 9, 2021 and April 2, 2021, most often for foreign ob (FOREIGN OB).

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

Current status

Import alerts: Not listed
Last import refusal: Apr 2, 2021Gel cups, fruit flavored · UNSAFE COL
Last warning letter: None found
Last inspection: None on record

Every FDA record for Eishindo

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

2021

Apr 2, 2021Import refusal
Refused, Gel cups, fruit flavoredUNSAFE COL FILTHYEntry 316-2565015-0
Source
Mar 31, 2021Import refusal
Refused, Gel cups, fruit flavoredUNSAFE COL FOREIGN OBEntry 316-2575927-4
Source
Feb 9, 2021Import refusal
Refused, Jellied candy, soft (jelly beans, gum drops, etc.), without nuts and fruit (without chocolate)FOREIGN OBEntry KL1-0248884-0
Source

Refusal charges, in plain English

FOREIGN OB2 refused lines
FOREIGN OB
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.
FILTHY1 refused line
Filthy, putrid or decomposed substance
The product appeared to consist in whole or in part of a filthy, putrid, or decomposed substance, or to be otherwise unfit for food.

Questions about Eishindo

Is Eishindo on an FDA import alert?: No listing for Eishindo appears in the FDA import alerts SupplierRadar checked on October 25, 2026. Country-wide alerts may still apply to its products; see the Japan page.
Has FDA refused shipments from Eishindo?: Yes. FDA refused 3 shipment lines from Eishindo between February 9, 2021 and April 2, 2021. The most recent, on April 2, 2021, was gel cups, fruit flavored, charged as UNSAFE COL (color additive unsafe under section 721).
Why did FDA refuse Eishindo's shipments?: The most frequent charges are FOREIGN OB (foreign ob, 2 lines) and UNSAFE COL (color additive unsafe under section 721, 2 lines).
What is Eishindo's FEI number?: Eishindo's FDA Establishment Identifier (FEI) is 3010124844.

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