SUCESORES DE BLAS PALOMARES SL
⚠️ High Risk
FEI: 3015352012 • Novelda, Alicante • SPAIN
FEI Number
3015352012
Location
Novelda, Alicante
Country
SPAINAddress
Avenida Jesus Navarro Jover, 19, , Novelda, Alicante, Spain
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
SALMONELLA
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain Salmonella, a poisonous and deleterious substance which may render it injurious to health.
FSVP VIO
The article is subject to refusal of admission pursuant to section 801(a)(3) of the Federal Food, Drug, and Cosmetic Act (FD&C Act) in that it appears that the importer (as defined in section 805 of the FD&C Act) is in violation of section 805.
LACKS FIRM
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)(1) of the FD&C Act in that the food is in package form and the label fails to bear the name and place of business of the manufacturer, packer, or distributor.
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.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 5/16/2024 | 28BGT15CORIANDER, GROUND, CRACKED (SPICE) | Division of Northern Border Imports (DNBI) | |
| 2/15/2024 | 28BGT15CORIANDER, GROUND, CRACKED (SPICE) | 9SALMONELLA | Division of Northern Border Imports (DNBI) |
| 1/23/2024 | 28BHT15CORIANDER, GROUND, CRACKED (SPICE) | 9SALMONELLA | Division of Northern Border Imports (DNBI) |
| 1/23/2024 | 28BHT15CORIANDER, GROUND, CRACKED (SPICE) | 9SALMONELLA | Division of Northern Border Imports (DNBI) |
| 7/17/2023 | 28AGT15CORIANDER, WHOLE (SPICE) | 9SALMONELLA | Division of Northern Border Imports (DNBI) |
| 2/24/2022 | 28AGT48THYME, WHOLE (SPICE) | 3886FSVP VIO | Division of Northern Border Imports (DNBI) |
| 2/24/2022 | 28AGT90OREGANO, WHOLE (SPICE) | 3886FSVP VIO | Division of Northern Border Imports (DNBI) |
| 2/24/2022 | 28AGT53ROSEMARY, WHOLE (SPICE) | 3886FSVP VIO | Division of Northern Border Imports (DNBI) |
| 2/24/2022 | 28AGT99WHOLE SPICE, N.E.C. | 3886FSVP VIO | Division of Northern Border Imports (DNBI) |
Frequently Asked Questions
What is SUCESORES DE BLAS PALOMARES SL's FDA import refusal history?
SUCESORES DE BLAS PALOMARES SL (FEI: 3015352012) has 9 FDA import refusal record(s) in our database, spanning from 2/24/2022 to 5/16/2024.
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. SUCESORES DE BLAS PALOMARES SL's FEI number is 3015352012.
What types of violations has SUCESORES DE BLAS PALOMARES SL received?
SUCESORES DE BLAS PALOMARES SL 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 SUCESORES DE BLAS PALOMARES SL come from?
All FDA import refusal data for SUCESORES DE BLAS PALOMARES SL 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.