A Tu Salud

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

Refusal charges, in plain English

• UNSAFE COL4 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 LBLG3 refused lines

  Artificial coloring not declared

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

Questions about A Tu Salud

Is A Tu Salud on an FDA import alert?

Yes. As of October 25, 2026, A Tu Salud is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for fried cactus snacks with chili cactus churritos with chipotle; ;fried cactus snacks with chili cactus churritos with chipotle; mango and guajillo chili pepper salsa; fried cactus snacks with chili cactus churritos with chipotle; mango and guajillo chili pepper salsa; FDA published the listing on April 20, 2018.

Has FDA refused shipments from A Tu Salud?

Yes. FDA refused 4 shipment lines from A Tu Salud between May 4, 2018 and April 23, 2020. The most recent, on April 23, 2020, was other bakery products, n.e.c., charged as UNSAFE COL (color additive unsafe under section 721).

Why did FDA refuse A Tu Salud's shipments?

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

What is A Tu Salud's FEI number?

A Tu Salud's FDA Establishment Identifier (FEI) is 3011568748.

Can shipments from A Tu Salud still enter the U.S.?

Shipments of fried cactus snacks with chili cactus churritos with chipotle; ;fried cactus snacks with chili cactus churritos with chipotle; mango and guajillo chili pepper salsa; fried cactus snacks with chili cactus churritos with chipotle; mango and guajillo chili pepper salsa from A Tu Salud 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).