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EXPORTACIONES 4 HERMANAS

⚠️ Moderate Risk

FEI: 3004677952 • PUEBLA, MX-PUE • MEXICO

FEI

FEI Number

3004677952

📍

Location

PUEBLA, MX-PUE

🇲🇽

Country

MEXICO
🏢

Address

3 SUR 10702 COL LOMA, ENCANTADA PUEBLA, PUEBLA, MX-PUE, Mexico

Moderate Risk

FDA Import Risk Assessment

40.8
LowModerateHighCritical

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

Statistics

11
Total Refusals
10
Unique Violations
5/30/2007
Latest Refusal
8/5/2004
Earliest Refusal

Score Breakdown

Violation Severity
62.1×40%
Refusal Volume
40.0×30%
Recency
0.0×20%
Frequency
39.1×10%
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

3243×

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)).

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).

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).

621×

NEEDS FCE

It appears the manufacturer is not registered as a low acid canned food or acidified food manufacturer pursuant to 21 CFR 108.25(c)(1) or 108.35(c)(1).

641×

YELLOW #5

The food appears to bear or contain the color additive FD & C Yellow No. 5, which is not declared on the label per 21 CFR 74.705(a)(c) under section 721.

831×

NO PROCESS

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the manufacturer's failure to file a scheduled process demonstrates that the product is not being manufactured under the mandatory provisions of 21 CFR Part 108 and therefore appears to have been manufactured, processed, or packed, under insanitary conditions whereby it may have been rendered injurious to health.

111×

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).

91×

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.

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.

4731×

LABELING

The article appears in violation of FPLA because of its placement, form and/or contents statement.

Refusal History

DateProductViolationsDivision
5/30/2007
24AWC14STRINGBEANS
473LABELING
New York District Office (NYK-DO)
5/30/2007
23YGT99NUTS OR EDIBLE SEEDS NOT MENTIONED ELSEWHERE, N.E.C.
324NO ENGLISH
New York District Office (NYK-DO)
3/23/2007
22KGT99OTHER FRUITS AND FRUIT PRODUCTS, OTHER FRUIT JUICES OR CONCENTRATES, N.E.C.
64YELLOW #5
New York District Office (NYK-DO)
3/23/2007
07BGT02CORN CHIPS, FRIED
11UNSAFE COL
New York District Office (NYK-DO)
3/13/2007
12CFC13CHEESE, HISPANIC/LATINO/MEXICAN STYLE, ALL VARIETIES, INCLUDING QUESO
9SALMONELLA
New York District Office (NYK-DO)
3/5/2007
12YGY99CHEESE AND CHEESE PRODUCTS, NOT ELSEWHERE MENTIONED, N.E.C.
324NO ENGLISH
New York District Office (NYK-DO)
3/5/2007
33HFT06FLAVORED CANDY, SOFT (LIVE SAVERS, ETC.), WITH COCONUT (WITHOUT CHOCOLATE)
324NO ENGLISH
New York District Office (NYK-DO)
3/5/2007
23KFT01PUMPKIN SEED (EDIBLE SEED)
260FALSE
New York District Office (NYK-DO)
1/12/2005
60SAZ99ANTACID, N.E.C.
118NOT LISTED
75UNAPPROVED
New York District Office (NYK-DO)
9/1/2004
24FCY07PEPPER, SWEET (FRUIT USED AS VEGETABLE)
62NEEDS FCE
83NO PROCESS
New York District Office (NYK-DO)
8/5/2004
60SAZ99ANTACID, N.E.C.
118NOT LISTED
75UNAPPROVED
New York District Office (NYK-DO)

Frequently Asked Questions

What is EXPORTACIONES 4 HERMANAS's FDA import refusal history?

EXPORTACIONES 4 HERMANAS (FEI: 3004677952) has 11 FDA import refusal record(s) in our database, spanning from 8/5/2004 to 5/30/2007.

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. EXPORTACIONES 4 HERMANAS's FEI number is 3004677952.

What types of violations has EXPORTACIONES 4 HERMANAS received?

EXPORTACIONES 4 HERMANAS has been cited for 10 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 EXPORTACIONES 4 HERMANAS come from?

All FDA import refusal data for EXPORTACIONES 4 HERMANAS 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.