Karen Nataly Jimenez Gonzalez

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

Refusal charges, in plain English

• PESTICIDE2 refused lines

  Pesticide chemical residue

  The product appeared to contain a pesticide chemical residue that makes it adulterated under section 402(a)(2)(B) of the FD&C Act, for example a residue above the U.S. tolerance or one with no U.S. tolerance for that food.

• LACKS FIRM1 refused line

  Manufacturer name and address missing

  The packaged product's label appeared not to show the name and place of business of the manufacturer, packer, or distributor.

• LACKS N/C1 refused line

  Net quantity statement missing

  The packaged food appeared not to carry an accurate statement of the quantity of contents, such as net weight, measure, or count, on its label.

• USUAL NAME1 refused line

  Common or usual name missing

  The label appeared not to show the common or usual name of the food.

Questions about Karen Nataly Jimenez Gonzalez

Is Karen Nataly Jimenez Gonzalez on an FDA import alert?

Yes. As of October 26, 2026, Karen Nataly Jimenez Gonzalez is on the red list of FDA Import Alert 99-05, “Raw agricultural products: pesticides”, for carrots; FDA published the listing on February 3, 2026.

Has FDA refused shipments from Karen Nataly Jimenez Gonzalez?

Yes. FDA refused 2 shipment lines from Karen Nataly Jimenez Gonzalez on February 3, 2026. The most recent, on February 3, 2026, was carrot (root & tuber vegetable), charged as PESTICIDE (pesticide chemical residue).

Why did FDA refuse Karen Nataly Jimenez Gonzalez's shipments?

The most frequent charges are PESTICIDE (pesticide chemical residue, 2 lines) and LACKS FIRM (manufacturer name and address missing, 1 line).

What is Karen Nataly Jimenez Gonzalez's FEI number?

Karen Nataly Jimenez Gonzalez's FDA Establishment Identifier (FEI) is 3017630094.

Can shipments from Karen Nataly Jimenez Gonzalez still enter the U.S.?

Shipments of carrots from Karen Nataly Jimenez Gonzalez can be detained without physical examination under Import Alert 99-05; 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).