Fruticola Pico Largo SPR de RL de CV
⚠️ High Risk
FEI: 3011913127 • Col. Centro, Chihuahua • MEXICO
FEI Number
3011913127
Location
Col. Centro, Chihuahua
Country
MEXICOAddress
Calle Guerrero Gran Vision Km 1.3, , Col. Centro, Chihuahua, Mexico
High Risk
FDA Import Risk Assessment
This firm has a significant history of FDA import refusals with notable violations.
Statistics
Score Breakdown
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
PESTICIDE
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain a pesticide chemical residue, which causes the article to be adulterated within the meaning of section 402(a)(2)(B) of the FD&C Act. Bears or contains:
SULFITELBL
The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be misbranded because 1) it appears to contain sulfites but the label fails to declare the presence of sulfites, a fact material to sulfite-sensitive individuals who must avoid the ingredient due to potential health consequences from its consumption, and 2) it appears the food is fabricated from two or more ingredients and the label does not list the common or usual name of each ingredient.
PESTICIDE2
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:
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.
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).
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
| Date | Product | Violations | Division |
|---|---|---|---|
| 6/11/2025 | 20QGB01APPLE, DRIED OR PASTE | 241PESTICIDE | Division of Southwest Imports (DSWI) |
| 6/5/2025 | 20QGB01APPLE, DRIED OR PASTE | 241PESTICIDE | Division of Southwest Imports (DSWI) |
| 2/20/2020 | 21TGH05MANGO, DRIED OR PASTE | Division of Southwest Imports (DSWI) | |
| 1/12/2016 | 20QGT01APPLE, DRIED OR PASTE | 3721PESTICIDE2 | Southwest Import District Office (SWI-DO) |
| 8/29/2008 | 24FHI08PEPPER, HOT, N.E.C. (FRUIT USED AS VEGETABLE) | Southwest Import District Office (SWI-DO) |
Frequently Asked Questions
What is Fruticola Pico Largo SPR de RL de CV's FDA import refusal history?
Fruticola Pico Largo SPR de RL de CV (FEI: 3011913127) has 5 FDA import refusal record(s) in our database, spanning from 8/29/2008 to 6/11/2025.
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. Fruticola Pico Largo SPR de RL de CV's FEI number is 3011913127.
What types of violations has Fruticola Pico Largo SPR de RL de CV received?
Fruticola Pico Largo SPR de RL de CV has been cited for 6 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 Fruticola Pico Largo SPR de RL de CV come from?
All FDA import refusal data for Fruticola Pico Largo SPR de RL de CV 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.