Di Carlo Limone
⚠️ Moderate Risk
FEI: 3005999085 • Treponti Di G • ITALY
FEI Number
3005999085
Location
Treponti Di G
Country
ITALYAddress
Baglio 83, , Treponti Di G, , Italy
Moderate Risk
FDA Import Risk Assessment
This firm has a moderate history of FDA import refusals. Some attention may be warranted.
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
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.
NO ENGLISH
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(f) of the FD&C Act in that any word, statement, or other information required by or under the authority of the FD&C Act to appear on the label or labeling is not prominently placed thereon with such conspicuousness (as compared with other words, statements, designs, or devices, in the labeling) and in such terms as to render it likely to be read and understood by the ordinary individual under customary terms of purchase and use (for example, label contains information in two or more languages but fails to repeat all required information in both languages in accordance with 21 CFR 101.15(c)(2), or label fails to include all required information in English in accordance with 21 CFR 101.15(c)(1), except in the case of articles distributed solely in the Commonwealth of Puerto Rico or in a Territory where the predominant language is one other than English)).
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.
USUAL NAME
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(i)(1) of the FD&C Act in that the label fails to bear the common or usual name of the food, if any there be.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 12/21/2006 | 37JCT08TOMATO SAUCE (WITH OTHER INGREDIENTS) | New Orleans District Office (NOL-DO) | |
| 12/21/2006 | 21HCT09OLIVES, DRIED OR PASTE | New Orleans District Office (NOL-DO) | |
| 12/21/2006 | 24HCT01EGG PLANT, DRIED OR PASTE | New Orleans District Office (NOL-DO) | |
| 12/21/2006 | 20RCT01APPLE, JAM, JELLY, PRESERVES, MARMALADE, BUTTER AND CANDIED | New Orleans District Office (NOL-DO) | |
| 12/21/2006 | 25LCT25ONION BULB (YELLOW, WHITE, RED, ETC.), DRIED OR PASTE | New Orleans District Office (NOL-DO) |
Frequently Asked Questions
What is Di Carlo Limone's FDA import refusal history?
Di Carlo Limone (FEI: 3005999085) has 5 FDA import refusal record(s) in our database, spanning from 12/21/2006 to 12/21/2006.
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. Di Carlo Limone's FEI number is 3005999085.
What types of violations has Di Carlo Limone received?
Di Carlo Limone has been cited for 4 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 Di Carlo Limone come from?
All FDA import refusal data for Di Carlo Limone 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.