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Hersan Helva Recel Gida Sanayi Ve Ticaret Anonim Sirketi

FDA import alert and refusal historyEsenyurt, TurkeyFEI 3030897254

Recorded by FDA as HERSAN HELVA RECEL GIDA SANAYI VE TICARET ANONIM SIRKETI

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Example subjectHersan Helva Recel Gida Sanayi Ve Ticaret Anonim Sirket added to Import Alert 16-129 (red list)

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As of October 27, 2026, Hersan Helva Recel Gida Sanayi Ve Ticaret Anonim Sirketi (Esenyurt, Turkey) is on the red list of FDA Import Alert 99-39 (Imported foods that appear to be misbranded) for pomegranate molasses, published by FDA on August 19, 2026, and has 2 FDA import refusals recorded since October 2016.

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

Current status

Last import refusal
Molasses · LIST INGRE
Last warning letter
None found
Last inspection
None on record

Every FDA record for Hersan Helva Recel Gida Sanayi Ve Ticaret Anonim Sirketi

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

2026

  1. Import refusal
    Refused, MolassesLIST INGREFILTHYFALSENO ENGLISHNUTRIT LBLEntry 417-0413158-4
    Source
  2. Import alert listing
    Listed on Import Alert 99-39red listPomegranate Molasses
    Source

2025

  1. Import refusal
    Refused, Currants, black, jam, jelly, preserves, marmalade, butter and candiedSULFITELBLINCONSPICUNUTRIT LBLEntry F23-9328380-9
    Source

Refusal charges, in plain English

  • NUTRIT LBL2 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.

  • FALSE1 refused line

    False or misleading labeling

    The labeling appeared to be false or misleading in some particular.

  • FILTHY1 refused line

    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.

  • INCONSPICU1 refused line

    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.

  • LIST INGRE1 refused line

    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).

  • NO ENGLISH1 refused line

    Required label information not in English

    Information that must appear on the label appeared not to be given in English, or not to be repeated in every language used on the label.

  • SULFITELBL1 refused line

    SULFITELBL

Questions about Hersan Helva Recel Gida Sanayi Ve Ticaret Anonim Sirketi

Is Hersan Helva Recel Gida Sanayi Ve Ticaret Anonim Sirketi on an FDA import alert?
Yes. As of October 27, 2026, Hersan Helva Recel Gida Sanayi Ve Ticaret Anonim Sirketi is on the red list of FDA Import Alert 99-39, “Imported foods that appear to be misbranded”, for pomegranate molasses; FDA published the listing on August 19, 2026.
Has FDA refused shipments from Hersan Helva Recel Gida Sanayi Ve Ticaret Anonim Sirketi?
Yes. FDA refused 2 shipment lines from Hersan Helva Recel Gida Sanayi Ve Ticaret Anonim Sirketi between February 20, 2025 and September 10, 2026. The most recent, on September 10, 2026, was molasses, charged as LIST INGRE (ingredients not listed).
Why did FDA refuse Hersan Helva Recel Gida Sanayi Ve Ticaret Anonim Sirketi's shipments?
The most frequent charges are NUTRIT LBL (nutrition information missing from label, 2 lines) and FALSE (false or misleading labeling, 1 line).
What is Hersan Helva Recel Gida Sanayi Ve Ticaret Anonim Sirketi's FEI number?
Hersan Helva Recel Gida Sanayi Ve Ticaret Anonim Sirketi's FDA Establishment Identifier (FEI) is 3030897254.
Can shipments from Hersan Helva Recel Gida Sanayi Ve Ticaret Anonim Sirketi still enter the U.S.?
Shipments of pomegranate molasses from Hersan Helva Recel Gida Sanayi Ve Ticaret Anonim Sirketi can be detained without physical examination under Import Alert 99-39; 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.