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KAWASHIMA HONKE

⚠️ Moderate Risk

FEI: 3010028080 • Wakayama, Wakayama • JAPAN

FEI

FEI Number

3010028080

📍

Location

Wakayama, Wakayama

🇯🇵

Country

JAPAN
🏢

Address

1757, Minato, Wakayama, Wakayama, Japan

Moderate Risk

FDA Import Risk Assessment

47.4
LowModerateHighCritical

This firm has a moderate history of FDA import refusals. Some attention may be warranted.

Statistics

7
Total Refusals
5
Unique Violations
5/16/2013
Latest Refusal
5/16/2013
Earliest Refusal

Score Breakdown

Violation Severity
76.0×40%
Refusal Volume
33.5×30%
Recency
0.0×20%
Frequency
70.0×10%
How is this score calculated?

Proprietary Algorithm

  • 40% Violation Severity — AI-assessed (1-10)
  • 30% Refusal Volume — Logarithmic scale
  • 20% Recency — Decays over 5 years
  • 10% Frequency — Refusals per year

© ImportRefusal.com Original Analysis

Violation Summary

117×

UNSAFE COL

The article appears to be, or to bear or contain a color additive which is unsafe within the meaning of Section 721(a).

2747×

COLOR LBLG

The article appears to contain an artificial coloring and it fails to bear labeling stating that fact.

3067×

INSANITARY

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to have been prepared, packed, or held under insanitary conditions whereby it may have become contaminated with filth, or whereby it may have been rendered injurious to health.

627×

NEEDS FCE

It appears the manufacturer is not registered as a low acid canned food or acidified food manufacturer pursuant to 21 CFR 108.25(c)(1) or 108.35(c)(1).

837×

NO PROCESS

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the manufacturer's failure to file a scheduled process demonstrates that the product is not being manufactured under the mandatory provisions of 21 CFR Part 108 and therefore appears to have been manufactured, processed, or packed, under insanitary conditions whereby it may have been rendered injurious to health.

Refusal History

DateProductViolationsDivision
5/16/2013
25JGT07RADISH (ROOT & TUBER VEGETABLE)
11UNSAFE COL
274COLOR LBLG
306INSANITARY
62NEEDS FCE
83NO PROCESS
Los Angeles District Office (LOS-DO)
5/16/2013
25JGT07RADISH (ROOT & TUBER VEGETABLE)
11UNSAFE COL
274COLOR LBLG
306INSANITARY
62NEEDS FCE
83NO PROCESS
Los Angeles District Office (LOS-DO)
5/16/2013
25JGT07RADISH (ROOT & TUBER VEGETABLE)
11UNSAFE COL
274COLOR LBLG
306INSANITARY
62NEEDS FCE
83NO PROCESS
Los Angeles District Office (LOS-DO)
5/16/2013
25JGT07RADISH (ROOT & TUBER VEGETABLE)
11UNSAFE COL
274COLOR LBLG
306INSANITARY
62NEEDS FCE
83NO PROCESS
Los Angeles District Office (LOS-DO)
5/16/2013
25JGT07RADISH (ROOT & TUBER VEGETABLE)
11UNSAFE COL
274COLOR LBLG
306INSANITARY
62NEEDS FCE
83NO PROCESS
Los Angeles District Office (LOS-DO)
5/16/2013
25JGT07RADISH (ROOT & TUBER VEGETABLE)
11UNSAFE COL
274COLOR LBLG
306INSANITARY
62NEEDS FCE
83NO PROCESS
Los Angeles District Office (LOS-DO)
5/16/2013
25JGT07RADISH (ROOT & TUBER VEGETABLE)
11UNSAFE COL
274COLOR LBLG
306INSANITARY
62NEEDS FCE
83NO PROCESS
Los Angeles District Office (LOS-DO)

Frequently Asked Questions

What is KAWASHIMA HONKE's FDA import refusal history?

KAWASHIMA HONKE (FEI: 3010028080) has 7 FDA import refusal record(s) in our database, spanning from 5/16/2013 to 5/16/2013.

What is an FEI number?

FEI stands for Firm Establishment Identifier. It's a unique number assigned by the FDA to identify establishments that manufacture, process, pack, or hold food, drugs, medical devices, or other FDA-regulated products. KAWASHIMA HONKE's FEI number is 3010028080.

What types of violations has KAWASHIMA HONKE received?

KAWASHIMA HONKE has been cited for 5 different violation type(s). Common FDA violations include adulteration (unsafe or unsanitary products), misbranding (incorrect or misleading labels), and regulatory non-compliance.

Where does this information about KAWASHIMA HONKE come from?

All FDA import refusal data for KAWASHIMA HONKE is sourced from the official FDA Data Dashboard (datadashboard.fda.gov), a public government database maintained by the U.S. Food and Drug Administration.

Data sourced from the FDA Data Dashboard, a public database maintained by the U.S. Food and Drug Administration.