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MONDELEZ MEXICO S DE RL D CV

⚠️ High Risk

FEI: 3017734755 • Puebla • MEXICO

FEI

FEI Number

3017734755

📍

Location

Puebla

🇲🇽

Country

MEXICO
🏢

Address

Av 18 De Noviembre # 1028, , Puebla, , Mexico

High Risk

FDA Import Risk Assessment

51.5
LowModerateHighCritical

This firm has a significant history of FDA import refusals with notable violations.

Statistics

7
Total Refusals
7
Unique Violations
9/29/2025
Latest Refusal
7/26/2023
Earliest Refusal

Score Breakdown

Violation Severity
55.5×40%
Refusal Volume
33.5×30%
Recency
80.0×20%
Frequency
32.1×10%
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

116×

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).

2745×

COLOR LBLG

The article appears to contain an artificial coloring and it fails to bear labeling stating that fact.

4823×

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.

2562×

INCONSPICU

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)).

3242×

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)).

2181×

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.

33001×

ALLERGEN

the label fails to declare all major food allergens present in the product, as required by section 403(w)(1).

Refusal History

DateProductViolationsDivision
9/29/2025
33UFT02CHEWING GUM (WITHOUT CHOCOLATE)
11UNSAFE COL
274COLOR LBLG
Division of Southeast Imports (DSEI)
9/29/2025
33UFT02CHEWING GUM (WITHOUT CHOCOLATE)
11UNSAFE COL
274COLOR LBLG
Division of Southeast Imports (DSEI)
1/7/2025
33UGD02CHEWING GUM (WITHOUT CHOCOLATE)
11UNSAFE COL
256INCONSPICU
482NUTRIT LBL
Division of Southwest Imports (DSWI)
11/26/2024
03HGT02CHOCOLATE PLAIN COOKIES,BISCUITS AND WAFERS
218LIST INGRE
256INCONSPICU
3300ALLERGEN
Division of Southwest Imports (DSWI)
5/7/2024
33UHT02CHEWING GUM (WITHOUT CHOCOLATE)
11UNSAFE COL
274COLOR LBLG
Division of Southwest Imports (DSWI)
7/26/2023
33UFT02CHEWING GUM (WITHOUT CHOCOLATE)
11UNSAFE COL
274COLOR LBLG
324NO ENGLISH
482NUTRIT LBL
Division of Southwest Imports (DSWI)
7/26/2023
33UFT02CHEWING GUM (WITHOUT CHOCOLATE)
11UNSAFE COL
274COLOR LBLG
324NO ENGLISH
482NUTRIT LBL
Division of Southwest Imports (DSWI)

Frequently Asked Questions

What is MONDELEZ MEXICO S DE RL D CV's FDA import refusal history?

MONDELEZ MEXICO S DE RL D CV (FEI: 3017734755) has 7 FDA import refusal record(s) in our database, spanning from 7/26/2023 to 9/29/2025.

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. MONDELEZ MEXICO S DE RL D CV's FEI number is 3017734755.

What types of violations has MONDELEZ MEXICO S DE RL D CV received?

MONDELEZ MEXICO S DE RL D CV has been cited for 7 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 MONDELEZ MEXICO S DE RL D CV come from?

All FDA import refusal data for MONDELEZ MEXICO S DE RL D CV 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.