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Industrias Del Mar Lubar Cia Ltd

⚠️ Moderate Risk

FEI: 3004124303 • Manta, Manabi • ECUADOR

FEI

FEI Number

3004124303

📍

Location

Manta, Manabi

🇪🇨

Country

ECUADOR
🏢

Address

Km 4.5 Via Manta-Portoviejo, , Manta, Manabi, Ecuador

Moderate Risk

FDA Import Risk Assessment

48.0
LowModerateHighCritical

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

Statistics

8
Total Refusals
5
Unique Violations
4/1/2010
Latest Refusal
5/28/2004
Earliest Refusal

Score Breakdown

Violation Severity
90.0×40%
Refusal Volume
35.3×30%
Recency
0.0×20%
Frequency
13.7×10%
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

2492×

FILTHY

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the article appears to consist in whole or in part of a filthy, putrid, or decomposed substance or be otherwise unfit for food.

25802×

MFRHACCP

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the Act in that it appears to have been prepared, packed or held under insanitary conditions whereby it may have been rendered injurious to health in that it appears to have been processed in violation of 21 CFR 123.6(a) and 123.8(a).

3082×

MFR INSAN

The article is subject to refusal of admission pursuant to section 801(a)(1) in that the article appears to have been manufactured, processed, or packed under insanitary conditions.

1811×

UNDER PRC

The article appears to have inadequate processing in having been prepared, packed, or held under insanitary conditions whereby it may have been rendered injurious to health.

23601×

HISTAMINE

The article appears to bear or contain histamine, a poisonous and deleterious substance in such quantity as ordinarily renders it injurious to health.

Refusal History

DateProductViolationsDivision
4/1/2010
16IEE33SARDINES (BRISLING, SPRATS, PILCHARDS, ETC.), HOT SMOKED, FISH
181UNDER PRC
Florida District Office (FLA-DO)
8/1/2007
16AEE33SARDINES (BRISLING, SPRATS, PILCHARDS, ETC.)
249FILTHY
Los Angeles District Office (LOS-DO)
5/25/2007
16AEE33SARDINES (BRISLING, SPRATS, PILCHARDS, ETC.)
2360HISTAMINE
Los Angeles District Office (LOS-DO)
5/11/2006
16AGC45TUNA (ALBACORE, YELLOWFIN, BLUEFIN, SKIPJACK, ETC.)
2580MFRHACCP
Florida District Office (FLA-DO)
5/11/2006
16AGC45TUNA (ALBACORE, YELLOWFIN, BLUEFIN, SKIPJACK, ETC.)
2580MFRHACCP
Florida District Office (FLA-DO)
5/11/2006
16AGT54MARLIN
308MFR INSAN
Florida District Office (FLA-DO)
2/24/2006
16AGT54MARLIN
308MFR INSAN
Florida District Office (FLA-DO)
5/28/2004
16AGC69ESCOLAR
249FILTHY
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is Industrias Del Mar Lubar Cia Ltd's FDA import refusal history?

Industrias Del Mar Lubar Cia Ltd (FEI: 3004124303) has 8 FDA import refusal record(s) in our database, spanning from 5/28/2004 to 4/1/2010.

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. Industrias Del Mar Lubar Cia Ltd's FEI number is 3004124303.

What types of violations has Industrias Del Mar Lubar Cia Ltd received?

Industrias Del Mar Lubar Cia Ltd 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 Industrias Del Mar Lubar Cia Ltd come from?

All FDA import refusal data for Industrias Del Mar Lubar Cia Ltd 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.