Quinta Generacion

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

Refusal charges, in plain English

• LACKS N/C3 refused lines

  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.

• 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.

• COLOR LBLG2 refused lines

  Artificial coloring not declared

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

• 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 Quinta Generacion

Is Quinta Generacion on an FDA import alert?

Yes. As of October 26, 2026, Quinta Generacion is on the red list of FDA Import Alert 99-08, “Processed human and animal foods: pesticides”, for raspberry jam; FDA published the listing on February 11, 2020.

Has FDA refused shipments from Quinta Generacion?

Yes. FDA refused 3 shipment lines from Quinta Generacion on February 5, 2020. The most recent, on February 5, 2020, was strawberry, jam, jelly, preserves, marmalade, butter and candied, charged as UNSAFE COL (color additive unsafe under section 721).

Why did FDA refuse Quinta Generacion's shipments?

The most frequent charges are LACKS N/C (net quantity statement missing, 3 lines) and UNSAFE COL (color additive unsafe under section 721, 3 lines).

What is Quinta Generacion's FEI number?

Quinta Generacion's FDA Establishment Identifier (FEI) is 3013643165.

Can shipments from Quinta Generacion still enter the U.S.?

Shipments of raspberry jam from Quinta Generacion can be detained without physical examination under Import Alert 99-08; 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).