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Gisela Judith Rodriguez Garcia

FDA import alert and refusal historyCadereyta Jimenez, MexicoFEI 3010111661

Recorded by FDA as GISELA JUDITH RODRIGUEZ GARCIA

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Example subjectGisela Judith Rodriguez Garci added to Import Alert 16-129 (red list)

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As of October 26, 2026, Gisela Judith Rodriguez Garcia (Cadereyta Jimenez, Mexico) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for mango pulp with chili manvaso, published by FDA on July 21, 2016, is also listed on Import Alert 99-21 (red list), and has 2 FDA import refusals recorded since October 2016.

Data from FDA public records, last checked . Request a correction

Current status

Last import refusal
Candy bar or pieces (not caramel or fondant), soft, with fruit (without chocolate) · UNSAFE COL
Last warning letter
None found
Last inspection
Classified VAI (Voluntary Action Indicated)

Every FDA record for Gisela Judith Rodriguez Garcia

5 records, newest first. Each line links to the FDA page it came from.

2023

  1. Import refusal
    Refused, Candy bar or pieces (not caramel or fondant), soft, with fruit (without chocolate)UNSAFE COLCOLOR LBLGEntry 8MH-0038676-9
    Source

2019

  1. Import refusal
    Refused, Candy bar or pieces (not caramel or fondant), soft, with coconut (without chocolate)FALSEEntry 8MH-0004021-8
    Source

2018

  1. Inspection
    Inspection classified VAI (Voluntary Action Indicated)Foodborne Biological Hazards
    Source

2016

  1. Import alert listing
    Listed on Import Alert 45-02red listMango Pulp with Chili Manvaso
    Source

2011

  1. Import alert listing
    Listed on Import Alert 99-21red listSweet Potato Candy
    Source

Refusal charges, in plain English

  • COLOR LBLG1 refused line

    Artificial coloring not declared

    The product appeared to contain an artificial coloring without labeling that states that fact.

  • FALSE1 refused line

    False or misleading labeling

    The labeling appeared to be false or misleading in some particular.

  • UNSAFE COL1 refused line

    Color additive unsafe under section 721

    The product appeared to be, or to contain, a color additive that is unsafe within the meaning of section 721(a) of the FD&C Act, the section that governs which color additives may be used and how.

Questions about Gisela Judith Rodriguez Garcia

Is Gisela Judith Rodriguez Garcia on an FDA import alert?
Yes. As of October 26, 2026, Gisela Judith Rodriguez Garcia is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for mango pulp with chili manvaso; FDA published the listing on July 21, 2016.
Has FDA refused shipments from Gisela Judith Rodriguez Garcia?
Yes. FDA refused 2 shipment lines from Gisela Judith Rodriguez Garcia between April 19, 2019 and April 21, 2023. The most recent, on April 21, 2023, was candy bar or pieces (not caramel or fondant), soft, with fruit (without chocolate), charged as UNSAFE COL (color additive unsafe under section 721).
Why did FDA refuse Gisela Judith Rodriguez Garcia's shipments?
The most frequent charges are COLOR LBLG (artificial coloring not declared, 1 line) and FALSE (false or misleading labeling, 1 line).
When was Gisela Judith Rodriguez Garcia last inspected by FDA?
FDA's most recent inspection of Gisela Judith Rodriguez Garcia with a final classification is dated October 19, 2018 and was classified VAI (Voluntary Action Indicated).
What is Gisela Judith Rodriguez Garcia's FEI number?
Gisela Judith Rodriguez Garcia's FDA Establishment Identifier (FEI) is 3010111661.
Can shipments from Gisela Judith Rodriguez Garcia still enter the U.S.?
Shipments of mango pulp with chili manvaso from Gisela Judith Rodriguez Garcia can be detained without physical examination under Import Alert 45-02; FDA releases them only if evidence shows they do not have the listed violation. Importers must consider this listing in their FSVP evaluation (21 CFR 1.505).

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Example subjectGisela Judith Rodriguez Garci added to Import Alert 16-129 (red list)

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SupplierRadar is not affiliated with the U.S. Food and Drug Administration. Data comes from public FDA records and may contain errors. This is not legal advice; importers remain responsible for their supplier evaluations.