Estefania Vilma Resendiz Jimenez

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

Refusal charges, in plain English

• COLOR LBLG4 refused lines

  Artificial coloring not declared

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

• UNSAFE COL3 refused lines

  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.

• FALSE1 refused line

  False or misleading labeling

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

Questions about Estefania Vilma Resendiz Jimenez

Is Estefania Vilma Resendiz Jimenez on an FDA import alert?

Yes. As of October 26, 2026, Estefania Vilma Resendiz Jimenez is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for marshmallow cones (barquillos con malvavisco); marshmallow cones barquillos con malvavisco; FDA published the listing on July 31, 2013.

Has FDA refused shipments from Estefania Vilma Resendiz Jimenez?

Yes. FDA refused 4 shipment lines from Estefania Vilma Resendiz Jimenez between December 14, 2016 and October 21, 2020. The most recent, on October 21, 2020, was candy specialties, n.e.c. (without chocolate), charged as FALSE (false or misleading labeling).

Why did FDA refuse Estefania Vilma Resendiz Jimenez's shipments?

The most frequent charges are COLOR LBLG (artificial coloring not declared, 4 lines) and UNSAFE COL (color additive unsafe under section 721, 3 lines).

What is Estefania Vilma Resendiz Jimenez's FEI number?

Estefania Vilma Resendiz Jimenez's FDA Establishment Identifier (FEI) is 3012262742.

Can shipments from Estefania Vilma Resendiz Jimenez still enter the U.S.?

Shipments of marshmallow cones (barquillos con malvavisco); marshmallow cones barquillos con malvavisco from Estefania Vilma Resendiz Jimenez 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).