Pescaradolc Srl

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

Refusal charges, in plain English

• INCONSPICU4 refused lines

  Required information not conspicuous

  Information required on the label appeared not to be placed prominently or conspicuously enough to be read and understood by an ordinary consumer.

• LABELING4 refused lines

  Fair Packaging and Labeling Act

  The package appeared not to meet the Fair Packaging and Labeling Act because of the placement, form, or contents of a required label statement.

• NUTRIT LBL4 refused lines

  Nutrition information missing from label

  The label or labeling appeared not to carry the nutrition information that U.S. law requires for the food.

• UNSAFE COL1 refused line

  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.

Questions about Pescaradolc Srl

Is Pescaradolc Srl on an FDA import alert?

Yes. As of October 26, 2026, Pescaradolc Srl is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for amaretti morbidi lamone (raspberry); FDA published the listing on October 22, 2024.

Has FDA refused shipments from Pescaradolc Srl?

Yes. FDA refused 5 shipment lines from Pescaradolc Srl between October 29, 2024 and June 4, 2025. The most recent, on June 4, 2025, was plain cookies,biscuits and wafers, n.e.c., charged as INCONSPICU (required information not conspicuous).

Why did FDA refuse Pescaradolc Srl's shipments?

The most frequent charges are INCONSPICU (required information not conspicuous, 4 lines) and LABELING (fair packaging and labeling act, 4 lines).

What is Pescaradolc Srl's FEI number?

Pescaradolc Srl's FDA Establishment Identifier (FEI) is 3010060272.

Can shipments from Pescaradolc Srl still enter the U.S.?

Shipments of amaretti morbidi lamone (raspberry) from Pescaradolc Srl 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).