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El Kawafel El Misrea

⚠️ Moderate Risk

FEI: 3003237054 • Shoubra • EGYPT

FEI

FEI Number

3003237054

📍

Location

Shoubra

🇪🇬

Country

EGYPT
🏢

Address

16 El Basha St, , Shoubra, , Egypt

Moderate Risk

FDA Import Risk Assessment

37.5
LowModerateHighCritical

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

Statistics

15
Total Refusals
12
Unique Violations
8/30/2011
Latest Refusal
4/12/2002
Earliest Refusal

Score Breakdown

Violation Severity
56.4×40%
Refusal Volume
44.6×30%
Recency
0.0×20%
Frequency
16.0×10%
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

3216×

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.

4826×

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.

3286×

USUAL NAME

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)(1) of the FD&C Act in that the label fails to bear the common or usual name of the food, if any there be.

2494×

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.

2183×

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.

29203×

PESTICIDES

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:

1182×

NOT LISTED

It appears the drug or device is not included in a list required by Section 510(j), or a notice or other information respecting it was not provided as required by section 510(j) or 510(k).

92×

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.

2381×

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.

161×

DIRECTIONS

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it is a device whose label appears to not bear adequate directions for use.

751×

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).

3201×

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.

Refusal History

DateProductViolationsDivision
8/30/2011
21WGT14TAMARIND, TOPPING OR SYRUP
249FILTHY
Chicago District Office (CHI-DO)
8/22/2011
66VBL99MISCELLANEOUS PATENT MEDICINES, ETC.
118NOT LISTED
16DIRECTIONS
75UNAPPROVED
Chicago District Office (CHI-DO)
7/8/2008
24TGH25SPINACH (LEAF & STEM VEGETABLE)
2920PESTICIDES
Chicago District Office (CHI-DO)
7/8/2008
24TGH25SPINACH (LEAF & STEM VEGETABLE)
2920PESTICIDES
Chicago District Office (CHI-DO)
1/8/2008
63HAK08CASTOR OIL (CATHARTIC)
118NOT LISTED
Chicago District Office (CHI-DO)
2/1/2007
02DGT02RICE, PLAIN (WHITE OR POLISHED) PROCESSED (PACKAGED)
321LACKS N/C
328USUAL NAME
482NUTRIT LBL
Baltimore District Office (BLT-DO)
2/1/2007
23KGH05MELON SEEDS (EDIBLE SEED)
321LACKS N/C
328USUAL NAME
482NUTRIT LBL
Baltimore District Office (BLT-DO)
2/1/2007
24BGH05FAVA BEAN, DRIED OR PASTE
218LIST INGRE
321LACKS N/C
328USUAL NAME
482NUTRIT LBL
Baltimore District Office (BLT-DO)
2/1/2007
02FGT07WHEAT, MILLED (CRUSHED, COARSE GROUND OR CRACKED)
218LIST INGRE
321LACKS N/C
328USUAL NAME
482NUTRIT LBL
Baltimore District Office (BLT-DO)
7/26/2005
28FGT99MIXED SPICE AND SEASONINGS, GROUND, CRACKED, WITHOUT SALT, N.E.C.
9SALMONELLA
Chicago District Office (CHI-DO)
7/8/2005
28BGT99SPICES, GROUND, CRACKED, ETC., N.E.C.
2920PESTICIDES
New York District Office (NYK-DO)
6/14/2005
21TGT14TAMARIND, DRIED OR PASTE
249FILTHY
Florida District Office (FLA-DO)
9/27/2004
21TFT14TAMARIND, DRIED OR PASTE
249FILTHY
Chicago District Office (CHI-DO)
4/2/2003
24TFH99LEAF & STEM VEGETABLES, N.E.C.
238UNSAFE ADD
249FILTHY
321LACKS N/C
328USUAL NAME
482NUTRIT LBL
Detroit District Office (DET-DO)
4/12/2002
24TGT99LEAF & STEM VEGETABLES, N.E.C.
218LIST INGRE
320LACKS FIRM
321LACKS N/C
328USUAL NAME
482NUTRIT LBL
9SALMONELLA
Baltimore District Office (BLT-DO)

Frequently Asked Questions

What is El Kawafel El Misrea's FDA import refusal history?

El Kawafel El Misrea (FEI: 3003237054) has 15 FDA import refusal record(s) in our database, spanning from 4/12/2002 to 8/30/2011.

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. El Kawafel El Misrea's FEI number is 3003237054.

What types of violations has El Kawafel El Misrea received?

El Kawafel El Misrea has been cited for 12 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 El Kawafel El Misrea come from?

All FDA import refusal data for El Kawafel El Misrea 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.