Carpe Diem Raisins
⚠️ High Risk
FEI: 2000025705 • Upington, Northern Cape • SOUTH AFRICA
FEI Number
2000025705
Location
Upington, Northern Cape
Country
SOUTH AFRICAAddress
Plot 18 Straussburg, , Upington, Northern Cape, South Africa
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
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:
FILTHY
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the article appears to consist in whole or in part of a filthy, putrid, or decomposed substance or be otherwise unfit for food.
POISONOUS
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain a poisonous or deleterious substance which may render the article injurious to health. Contains:
UNSAFE ADD
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain an unsafe food additive within the meaning of section 409.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 5/2/2023 | 20AGT10RAISINS (DRIED GRAPES) (BERRY) | 249FILTHY | Division of Northeast Imports (DNEI) |
| 5/2/2023 | 20AGT10RAISINS (DRIED GRAPES) (BERRY) | 249FILTHY | Division of Northeast Imports (DNEI) |
| 11/23/2022 | 20AGT10RAISINS (DRIED GRAPES) (BERRY) | 249FILTHY | Division of Northeast Imports (DNEI) |
| 10/14/2022 | 20AGT10RAISINS (DRIED GRAPES) (BERRY) | 238UNSAFE ADD | Division of Northeast Imports (DNEI) |
| 2/27/2013 | 20AGT10RAISINS (DRIED GRAPES) (BERRY) | 3721PESTICIDE2 | New York District Office (NYK-DO) |
| 2/14/2013 | 20AGH10RAISINS (DRIED GRAPES) (BERRY) | 3721PESTICIDE2 | New York District Office (NYK-DO) |
| 1/30/2013 | 20AGT10RAISINS (DRIED GRAPES) (BERRY) | 3721PESTICIDE2 | New York District Office (NYK-DO) |
| 1/30/2013 | 20AGT10RAISINS (DRIED GRAPES) (BERRY) | 3721PESTICIDE2 | New York District Office (NYK-DO) |
| 1/7/2013 | 20AHT10RAISINS (DRIED GRAPES) (BERRY) | 251POISONOUS | New York District Office (NYK-DO) |
| 1/7/2013 | 20AGH10RAISINS (DRIED GRAPES) (BERRY) | 3721PESTICIDE2 | New York District Office (NYK-DO) |
| 12/20/2012 | 20AGT10RAISINS (DRIED GRAPES) (BERRY) | 3721PESTICIDE2 | New York District Office (NYK-DO) |
| 10/15/2012 | 20AGH10RAISINS (DRIED GRAPES) (BERRY) | 3721PESTICIDE2 | New York District Office (NYK-DO) |
| 10/9/2012 | 20AGH10RAISINS (DRIED GRAPES) (BERRY) | 251POISONOUS | New York District Office (NYK-DO) |
Frequently Asked Questions
What is Carpe Diem Raisins's FDA import refusal history?
Carpe Diem Raisins (FEI: 2000025705) has 13 FDA import refusal record(s) in our database, spanning from 10/9/2012 to 5/2/2023.
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. Carpe Diem Raisins's FEI number is 2000025705.
What types of violations has Carpe Diem Raisins received?
Carpe Diem Raisins 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 Carpe Diem Raisins come from?
All FDA import refusal data for Carpe Diem Raisins 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.