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Materne - Confilux

⚠️ Moderate Risk

FEI: 3002824770 • Floreffe, Namur • BELGIUM

FEI

FEI Number

3002824770

📍

Location

Floreffe, Namur

🇧🇪

Country

BELGIUM
🏢

Address

Allee des Cerisiers 1, , Floreffe, Namur, Belgium

Moderate Risk

FDA Import Risk Assessment

44.0
LowModerateHighCritical

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

Statistics

3
Total Refusals
5
Unique Violations
8/23/2024
Latest Refusal
2/10/2011
Earliest Refusal

Score Breakdown

Violation Severity
64.0×40%
Refusal Volume
22.3×30%
Recency
57.2×20%
Frequency
2.2×10%
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

29201×

PESTICIDES

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be adulterated because it contains a pesticide chemical, which is in violation of section 402(a)(2)(B). Contains:

3201×

LACKS FIRM

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(e)(1) of the FD&C Act in that the food is in package form and the label fails to bear the name and place of business of the manufacturer, packer, or distributor.

4821×

NUTRIT LBL

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be misbranded in that the label or labeling fails to bear the required nutrition information.

621×

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).

831×

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
8/23/2024
21CYT09OTHER FRUITS, MIXED, FLAVORED JAMS, JELLIES, PRESERVES, MARMALADES, BUTTERS AND CANDIED
62NEEDS FCE
83NO PROCESS
Division of Southeast Imports (DSEI)
2/4/2016
20UGT01APPLE (CORE FRUIT PUREES)
320LACKS FIRM
482NUTRIT LBL
New York District Office (NYK-DO)
2/10/2011
20CCT13RASPBERRY, RED, JAM, JELLY, PRESERVES, MARMALADE, BUTTER AND CANDIED
2920PESTICIDES
Southwest Import District Office (SWI-DO)

Frequently Asked Questions

What is Materne - Confilux's FDA import refusal history?

Materne - Confilux (FEI: 3002824770) has 3 FDA import refusal record(s) in our database, spanning from 2/10/2011 to 8/23/2024.

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. Materne - Confilux's FEI number is 3002824770.

What types of violations has Materne - Confilux received?

Materne - Confilux 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 Materne - Confilux come from?

All FDA import refusal data for Materne - Confilux 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.