J.Kahan Ltd.
⚠️ Moderate Risk
FEI: 3010045223 • Milouot • ISRAEL
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
UNSAFE COL
The article appears to be, or to bear or contain a color additive which is unsafe within the meaning of Section 721(a).
TRANSFAT
The product is misbranded under Section 403(q) because the nutrition label does not provide all of the information required by 21 CFR 101.9(c); specifically, the label does not bear the amount of trans fat [21 CFR 101.9(c)(2)(ii)].
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.
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 |
|---|---|---|---|
| 12/29/2020 | 30BHT01BEVERAGE BASE, BERRY, LIQUID | 11UNSAFE COL | Division of Southeast Imports (DSEI) |
| 4/1/2016 | 38CGT99DRIED SOUP, N.E.C. | Division of Northeast Imports (DNEI) | |
| 4/1/2016 | 38PCT19MUSHROOM BROTH, DRIED | Division of Northeast Imports (DNEI) | |
| 4/1/2016 | 38YFT99SOUP, N.E.C. | 238UNSAFE ADD | Division of Northeast Imports (DNEI) |
| 11/14/2014 | 35AGT01GELATIN, FLAVORED | 11UNSAFE COL | Los Angeles District Office (LOS-DO) |
Frequently Asked Questions
What is J.Kahan Ltd.'s FDA import refusal history?
J.Kahan Ltd. (FEI: 3010045223) has 5 FDA import refusal record(s) in our database, spanning from 11/14/2014 to 12/29/2020.
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. J.Kahan Ltd.'s FEI number is 3010045223.
What types of violations has J.Kahan Ltd. received?
J.Kahan Ltd. 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 J.Kahan Ltd. come from?
All FDA import refusal data for J.Kahan Ltd. 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.