Frantoi Cutrera
⚠️ Moderate Risk
FEI: 3004302148 • Chiaramonte Gulfi, Ragusa • ITALY
FEI Number
3004302148
Location
Chiaramonte Gulfi, Ragusa
Country
ITALYAddress
Contrada Piano Dell'Acqua 71, , Chiaramonte Gulfi, Ragusa, 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
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:
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.
LACKS N/C
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)(2) of the FD&C Act in that the food is in package form and the label fails to bear an accurate statement of the quantity of the contents in terms of weight, measure, or numerical count in accordance with Section 403(e)(2) of the FD&C Act.
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.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 6/18/2015 | 26ACE09VIRGIN OLIVE OIL, CRUDE | 3721PESTICIDE2 | Division of Northern Border Imports (DNBI) |
| 6/18/2015 | 26ACE09VIRGIN OLIVE OIL, CRUDE | 3721PESTICIDE2 | Division of Northern Border Imports (DNBI) |
| 6/18/2015 | 26ACE09VIRGIN OLIVE OIL, CRUDE | 3721PESTICIDE2 | Division of Northern Border Imports (DNBI) |
| 6/4/2015 | 26CCT04OLIVE OIL, REFINED, SINGLE INGREDIENT | 3721PESTICIDE2 | Los Angeles District Office (LOS-DO) |
| 5/18/2015 | 26ACY09VIRGIN OLIVE OIL, CRUDE | 3721PESTICIDE2 | New England District Office (NWE-DO) |
| 5/18/2015 | 26ACY09VIRGIN OLIVE OIL, CRUDE | 3721PESTICIDE2 | New England District Office (NWE-DO) |
| 5/13/2015 | 26ACT09VIRGIN OLIVE OIL, CRUDE | 3721PESTICIDE2 | Division of Northeast Imports (DNEI) |
| 5/13/2015 | 26ACT09VIRGIN OLIVE OIL, CRUDE | 3721PESTICIDE2 | Division of Northeast Imports (DNEI) |
| 5/13/2015 | 26ACT09VIRGIN OLIVE OIL, CRUDE | 3721PESTICIDE2 | Division of Northeast Imports (DNEI) |
| 1/26/2015 | 26ACT09VIRGIN OLIVE OIL, CRUDE | Detroit District Office (DET-DO) | |
| 1/26/2015 | 26ACT09VIRGIN OLIVE OIL, CRUDE | Detroit District Office (DET-DO) | |
| 2/9/2011 | 16ACT33SARDINES (BRISLING, SPRATS, PILCHARDS, ETC.) | New York District Office (NYK-DO) | |
| 2/9/2011 | 16ACT79YELLOWTAIL, AMBERJACK | New York District Office (NYK-DO) | |
| 2/9/2011 | 16ACT33SARDINES (BRISLING, SPRATS, PILCHARDS, ETC.) | New York District Office (NYK-DO) | |
| 2/9/2011 | 24KCT01EGG PLANT, WITH SAUCE | New York District Office (NYK-DO) | |
| 2/9/2011 | 16ACT45TUNA (ALBACORE, YELLOWFIN, BLUEFIN, SKIPJACK, ETC.) | New York District Office (NYK-DO) | |
| 2/9/2011 | 16ACT45TUNA (ALBACORE, YELLOWFIN, BLUEFIN, SKIPJACK, ETC.) | New York District Office (NYK-DO) | |
| 2/9/2011 | 16ACT45TUNA (ALBACORE, YELLOWFIN, BLUEFIN, SKIPJACK, ETC.) | New York District Office (NYK-DO) |
Frequently Asked Questions
What is Frantoi Cutrera's FDA import refusal history?
Frantoi Cutrera (FEI: 3004302148) has 18 FDA import refusal record(s) in our database, spanning from 2/9/2011 to 6/18/2015.
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. Frantoi Cutrera's FEI number is 3004302148.
What types of violations has Frantoi Cutrera received?
Frantoi Cutrera 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 Frantoi Cutrera come from?
All FDA import refusal data for Frantoi Cutrera 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.