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E.M.B YARDEN AGRICULTURAL FARM LTD

⚠️ Moderate Risk

FEI: 3006705704 • Beit Shemesh, Hamerkaz • ISRAEL

FEI

FEI Number

3006705704

📍

Location

Beit Shemesh, Hamerkaz

🇮🇱

Country

ISRAEL
🏢

Address

1, Ha-Oman, , Beit Shemesh, Hamerkaz, Israel

Moderate Risk

FDA Import Risk Assessment

47.8
LowModerateHighCritical

This firm has a moderate history of FDA import refusals. Some attention may be warranted.

Statistics

5
Total Refusals
8
Unique Violations
8/4/2025
Latest Refusal
9/25/2020
Earliest Refusal

Score Breakdown

Violation Severity
57.0×40%
Refusal Volume
28.8×30%
Recency
76.7×20%
Frequency
10.3×10%
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

2182×

LIST INGRE

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)(2) of the FD&C Act in that it is fabricated from two or more ingredients and the label fails to bear the common or usual name of each such ingredient and/or the article purports to be a beverage containing vegetable or fruit juice, but does not bear a statement with appropriate prominence on the information panel of the total percentage of such fruit or vegetable juice contained in the food.

752×

UNAPPROVED

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a new drug within the meaning of Section 201(p) without an approved New Drug Application (NDA).

2531×

STD IDENT

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(g)(1) of the FD&C Act in that the article purports to be or is represented as a food for which a definition and standard of identity have been prescribed by regulations as provided by section 401 of the FD&C Act and the article does not conform to such definition and standard.

2601×

FALSE

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(a)(1 ) of the FD&C Act in that the labeling is false or misleading in any particular.

3081×

MFR INSAN

The article is subject to refusal of admission pursuant to section 801(a)(1) in that the article appears to have been manufactured, processed, or packed under insanitary conditions.

3241×

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)).

4821×

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.

22801×

DIRSEXMPT

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a drug within the meaning of Section 201(g) and it lacks adequate directions for use.

Refusal History

DateProductViolationsDivision
8/4/2025
54KBY08ALOE (HERBAL AND BOTANICAL (NOT TEAS) II (CONTINUED))
218LIST INGRE
2280DIRSEXMPT
Division of Northern Border Imports (DNBI)
5/2/2025
41YCY99DIETARY CONVENTIONAL FOODS, N.E.C.
308MFR INSAN
75UNAPPROVED
Division of Southeast Imports (DSEI)
12/20/2024
54FEI99HERBALS & BOTANICALS (NOT TEAS), N.E.C.
218LIST INGRE
260FALSE
482NUTRIT LBL
75UNAPPROVED
Division of Southwest Imports (DSWI)
3/29/2023
54KYR08ALOE (HERBAL AND BOTANICAL (NOT TEAS) II (CONTINUED))
253STD IDENT
Division of Southeast Imports (DSEI)
9/25/2020
54YYY99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C.
324NO ENGLISH
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is E.M.B YARDEN AGRICULTURAL FARM LTD's FDA import refusal history?

E.M.B YARDEN AGRICULTURAL FARM LTD (FEI: 3006705704) has 5 FDA import refusal record(s) in our database, spanning from 9/25/2020 to 8/4/2025.

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. E.M.B YARDEN AGRICULTURAL FARM LTD's FEI number is 3006705704.

What types of violations has E.M.B YARDEN AGRICULTURAL FARM LTD received?

E.M.B YARDEN AGRICULTURAL FARM LTD has been cited for 8 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 E.M.B YARDEN AGRICULTURAL FARM LTD come from?

All FDA import refusal data for E.M.B YARDEN AGRICULTURAL FARM 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.