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EMPACADORA LA ROSITA

⚠️ Moderate Risk

FEI: 3004386385 • reynosa, MX-TAM • MEXICO

FEI

FEI Number

3004386385

📍

Location

reynosa, MX-TAM

🇲🇽

Country

MEXICO
🏢

Address

Calle Santa Cecilia No. 402, , reynosa, MX-TAM, Mexico

Moderate Risk

FDA Import Risk Assessment

49.7
LowModerateHighCritical

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

Statistics

3
Total Refusals
1
Unique Violations
10/19/2007
Latest Refusal
10/17/2007
Earliest Refusal

Score Breakdown

Violation Severity
100.0×40%
Refusal Volume
22.3×30%
Recency
0.0×20%
Frequency
30.0×10%
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

2953×

LISTERIA

The article is subject to refusal of admission pursuant to Section 801(a)(3), in that the article appears to contain Listeria monocytogenes, a poisonous and deleterious substance, which may render it injurious to health.

Refusal History

DateProductViolationsDivision
10/19/2007
21HGC02AVOCADO, DRIED OR PASTE
295LISTERIA
Southwest Import District Office (SWI-DO)
10/19/2007
21HGC02AVOCADO, DRIED OR PASTE
295LISTERIA
Southwest Import District Office (SWI-DO)
10/17/2007
21HGC02AVOCADO, DRIED OR PASTE
295LISTERIA
Southwest Import District Office (SWI-DO)

Frequently Asked Questions

What is EMPACADORA LA ROSITA's FDA import refusal history?

EMPACADORA LA ROSITA (FEI: 3004386385) has 3 FDA import refusal record(s) in our database, spanning from 10/17/2007 to 10/19/2007.

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. EMPACADORA LA ROSITA's FEI number is 3004386385.

What types of violations has EMPACADORA LA ROSITA received?

EMPACADORA LA ROSITA has been cited for 1 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 EMPACADORA LA ROSITA come from?

All FDA import refusal data for EMPACADORA LA ROSITA 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.