Carletti A/S

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

Refusal charges, in plain English

• UNSAFE COL2 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 LBLG1 refused line

  Artificial coloring not declared

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

Questions about Carletti A/S

Is Carletti A/S on an FDA import alert?

Yes. As of October 26, 2026, Carletti A/S is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for licorice candy, hard, without nuts and fruit (without chocolate); salte sild; licorice candy, soft, without nuts and fruit (without chocolate); FDA published the listing on September 18, 2009.

Has FDA refused shipments from Carletti A/S?

Yes. FDA refused 2 shipment lines from Carletti A/S between August 2, 2022 and August 26, 2022. The most recent, on August 26, 2022, was licorice candy, soft, without nuts and fruit (without chocolate), charged as UNSAFE COL (color additive unsafe under section 721).

Why did FDA refuse Carletti A/S's shipments?

The most frequent charges are UNSAFE COL (color additive unsafe under section 721, 2 lines) and COLOR LBLG (artificial coloring not declared, 1 line).

When was Carletti A/S last inspected by FDA?

FDA's most recent inspection of Carletti A/S with a final classification is dated August 14, 2012 and was classified VAI (Voluntary Action Indicated).

What is Carletti A/S's FEI number?

Carletti A/S's FDA Establishment Identifier (FEI) is 1000423405.

Can shipments from Carletti A/S still enter the U.S.?

Shipments of licorice candy, hard, without nuts and fruit (without chocolate); salte sild; licorice candy, soft, without nuts and fruit (without chocolate) from Carletti A/S 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).