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Campo d"Oro S.r.l.

FDA import alert and refusal historySciacca, ItalyFEI 3004308807

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Example subjectCampo d"Oro S.r.l added to Import Alert 16-129 (red list)

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As of October 26, 2026, Campo d"Oro S.r.l. (Sciacca, Italy) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for olives in brine, published by FDA on September 19, 2017, and has 11 FDA import refusals recorded since October 2016.

Data from FDA public records, last checked . Request a correction

Current status

Last import refusal
Olives, green, (pit fruit) · UNSAFE COL
Last warning letter
None found
Last inspection
Classified VAI (Voluntary Action Indicated)

Every FDA record for Campo d"Oro S.r.l.

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

2026

  1. Import refusal
    Refused, Olives, green, (pit fruit)UNSAFE COLCOLOR LBLGEntry 97N-0647434-1
    Source

2023

  1. Import refusal
    Refused, Olives, green, (pit fruit)UNSAFE COLEntry NWB-2201315-5
    Source

2020

  1. Import refusal
    Refused, Olives, green, (pit fruit)UNSAFE COLEntry 603-1112581-3
    Source
  2. Import refusal
    Refused, 2 lines in one entry: Olives, green, (pit fruit)UNSAFE COLEntry 603-1112629-0Show 2 lines
    Source

2019

  1. Import refusal
    Refused, Olives, green, (pit fruit)UNSAFE COLEntry DF4-0123397-1
    Source
  2. Import refusal
    Refused, Olives, green, (pit fruit)UNSAFE COLEntry DF4-0122333-7
    Source
  3. Import refusal
    Refused, Olives, green, (pit fruit)UNSAFE COLEntry DF4-0121266-0
    Source
  4. Import refusal
    Refused, Olives, green, (pit fruit)UNSAFE COLEntry 235-2339690-3
    Source

2017

  1. Import refusal
    Refused, 2 lines in one entry: Olives, green, (pit fruit)UNSAFE COLEntry DF4-0386830-3Show 2 lines
    Source
  2. Import alert listing
    Listed on Import Alert 45-02red listOlives in brine
    Source

2016

  1. Inspection
    Inspection classified VAI (Voluntary Action Indicated)Foodborne Biological Hazards
    Source

2011

  1. Inspection
    Inspection classified VAI (Voluntary Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological Hazards
    Source

2010

  1. Inspection
    Inspection classified OAI (Official Action Indicated)Foodborne Biological Hazards
    Source

Refusal charges, in plain English

  • UNSAFE COL11 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 Campo d"Oro S.r.l.

Is Campo d"Oro S.r.l. on an FDA import alert?
Yes. As of October 26, 2026, Campo d"Oro S.r.l. is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for olives in brine; FDA published the listing on September 19, 2017.
Has FDA refused shipments from Campo d"Oro S.r.l.?
Yes. FDA refused 11 shipment lines from Campo d"Oro S.r.l. between November 7, 2017 and June 2, 2026. The most recent, on June 2, 2026, was olives, green, (pit fruit), charged as UNSAFE COL (color additive unsafe under section 721).
Why did FDA refuse Campo d"Oro S.r.l.'s shipments?
The most frequent charges are UNSAFE COL (color additive unsafe under section 721, 11 lines) and COLOR LBLG (artificial coloring not declared, 1 line).
When was Campo d"Oro S.r.l. last inspected by FDA?
FDA's most recent inspection of Campo d"Oro S.r.l. with a final classification is dated January 20, 2016 and was classified VAI (Voluntary Action Indicated).
What is Campo d"Oro S.r.l.'s FEI number?
Campo d"Oro S.r.l.'s FDA Establishment Identifier (FEI) is 3004308807.
Can shipments from Campo d"Oro S.r.l. still enter the U.S.?
Shipments of olives in brine from Campo d"Oro S.r.l. 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).

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SupplierRadar is not affiliated with the U.S. Food and Drug Administration. Data comes from public FDA records and may contain errors. This is not legal advice; importers remain responsible for their supplier evaluations.