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Prodisabor SAS

FDA import alert and refusal historyBarranquilla, ColombiaFEI 3009808664

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Example subjectProdisabor SA added to Import Alert 16-129 (red list)

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As of October 25, 2026, Prodisabor SAS is not on any FDA import alert in SupplierRadar's records; FDA refused 5 of its shipment lines on April 21, 2023, most often for artificial coloring not declared (COLOR LBLG).

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

Current status

Import alerts
Not listed
Last import refusal
Vanilla (vanillin) imitation flavor · LIST INGRE
Last warning letter
None found
Last inspection
None on record

Every FDA record for Prodisabor SAS

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

2023

  1. Import refusal
    Refused, 5 lines in one entry: Vanilla (vanillin) imitation flavor; Passion fruit (subtropical and tropical fruit purees) and 2 moreLIST INGRECOLOR LBLGLACKS N/CCOLORLABELEntry DSV-9103495-6Show 5 lines
    Source

Refusal charges, in plain English

  • COLOR LBLG5 refused lines

    Artificial coloring not declared

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

  • COLORLABEL5 refused lines

    Required information not prominent

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

  • LACKS N/C5 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.

  • LIST INGRE5 refused lines

    Ingredients not listed

    The product is made from two or more ingredients and the label appeared not to list the common or usual name of each one (or, for a juice beverage, the percentage of juice).

  • NUTRIT LBL5 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.

Questions about Prodisabor SAS

Is Prodisabor SAS on an FDA import alert?
No listing for Prodisabor SAS appears in the FDA import alerts SupplierRadar checked on October 25, 2026. Country-wide alerts may still apply to its products; see the Colombia page.
Has FDA refused shipments from Prodisabor SAS?
Yes. FDA refused 5 shipment lines from Prodisabor SAS on April 21, 2023. The most recent, on April 21, 2023, was vanilla (vanillin) imitation flavor, charged as LIST INGRE (ingredients not listed).
Why did FDA refuse Prodisabor SAS's shipments?
The most frequent charges are COLOR LBLG (artificial coloring not declared, 5 lines) and COLORLABEL (required information not prominent, 5 lines).
What is Prodisabor SAS's FEI number?
Prodisabor SAS's FDA Establishment Identifier (FEI) is 3009808664.

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Example subjectProdisabor SA added to Import Alert 16-129 (red list)

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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.