Diana Estefania Jimenez Sanchez

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

Refusal charges, in plain English

• 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.

• PESTICIDE1 refused line

  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.

Questions about Diana Estefania Jimenez Sanchez

Is Diana Estefania Jimenez Sanchez on an FDA import alert?

Yes. As of October 26, 2026, Diana Estefania Jimenez Sanchez is on the red list of FDA Import Alert 99-05, “Raw agricultural products: pesticides”, for scallions (cebollita); FDA published the listing on January 30, 2024.

Has FDA refused shipments from Diana Estefania Jimenez Sanchez?

Yes. FDA refused 1 shipment line from Diana Estefania Jimenez Sanchez on January 5, 2024. The most recent, on January 5, 2024, was scallions, green onions (root & tuber vegetable), charged as PESTICIDE (pesticide chemical residue).

Why did FDA refuse Diana Estefania Jimenez Sanchez's shipments?

The most frequent charges are LACKS FIRM (manufacturer name and address missing, 1 line) and LACKS N/C (net quantity statement missing, 1 line).

What is Diana Estefania Jimenez Sanchez's FEI number?

Diana Estefania Jimenez Sanchez's FDA Establishment Identifier (FEI) is 3027989224.

Can shipments from Diana Estefania Jimenez Sanchez still enter the U.S.?

Shipments of scallions (cebollita) from Diana Estefania Jimenez Sanchez 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).