Demar Di Pesare F. & C. SRL

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

Refusal charges, in plain English

• FILTHY2 refused lines

  Filthy, putrid or decomposed substance

  The product appeared to consist in whole or in part of a filthy, putrid, or decomposed substance, or to be otherwise unfit for food.

• LACKS N/C2 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.

• SALMONELLA1 refused line

  Salmonella

  The product appeared to contain Salmonella, which the law treats as a poisonous and deleterious substance that may make food injurious to health.

Questions about Demar Di Pesare F. & C. SRL

Is Demar Di Pesare F. & C. SRL on an FDA import alert?

Yes. As of October 26, 2026, Demar Di Pesare F. & C. SRL is on the red list of FDA Import Alert 99-19, “Food products: Salmonella”, for dried elderberries; FDA published the listing on February 14, 2025.

Has FDA refused shipments from Demar Di Pesare F. & C. SRL?

Yes. FDA refused 3 shipment lines from Demar Di Pesare F. & C. SRL between April 16, 2019 and June 10, 2026. The most recent, on June 10, 2026, was berries, dried or paste, n.e.c., charged as FILTHY (filthy, putrid or decomposed substance).

Why did FDA refuse Demar Di Pesare F. & C. SRL's shipments?

The most frequent charges are FILTHY (filthy, putrid or decomposed substance, 2 lines) and LACKS N/C (net quantity statement missing, 2 lines).

When was Demar Di Pesare F. & C. SRL last inspected by FDA?

FDA's most recent inspection of Demar Di Pesare F. & C. SRL with a final classification is dated October 28, 2024 and was classified NAI (No Action Indicated).

What is Demar Di Pesare F. & C. SRL's FEI number?

Demar Di Pesare F. & C. SRL's FDA Establishment Identifier (FEI) is 3008587894.

Can shipments from Demar Di Pesare F. & C. SRL still enter the U.S.?

Shipments of dried elderberries from Demar Di Pesare F. & C. SRL can be detained without physical examination under Import Alert 99-19; 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).