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Herbalart Gida San Ve Tic Ltd

FDA import alert and refusal historyIzmit, TurkeyFEI 3015909758

Recorded by FDA as HERBALART GIDA SAN VE TIC LTD

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Example subjectHerbalart Gida San Ve Tic Lt added to Import Alert 16-129 (red list)

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As of October 26, 2026, Herbalart Gida San Ve Tic Ltd (Izmit, Turkey) is on the red list of FDA Import Alert 54-16 (Foods/supplements with active pharmaceutical ingredient) for stamina by honey- honey mixed herbal paste (aka epimedium mixed herbal paste), published by FDA on December 11, 2020, 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
Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c. · NO ENGLISH
Last warning letter
None found
Last inspection
None on record

Every FDA record for Herbalart Gida San Ve Tic Ltd

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

2022

  1. Import refusal
    Refused, Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.NO ENGLISHNUTRIT LBLEntry 799-1634219-9
    Source

2020

  1. Import alert listing
    Listed on Import Alert 54-16red listStamina By Honey- Honey Mixed Herbal Paste (aka Epimedium Mixed Herbal Paste)
    Source
  2. Import refusal
    Refused, Herbals & botanicals (not teas), n.e.c.LIST INGREUNAPPROVEDEntry 9XB-0010628-0
    Source

Refusal charges, in plain English

  • 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.

  • NUTRIT LBL1 refused line

    Nutrition information missing from label

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

  • UNAPPROVED1 refused line

    Unapproved new drug

    The product appeared to be a new drug within the meaning of section 201(p) of the FD&C Act without an approved New Drug Application. FDA can apply this charge to a food or supplement whose labeling presents it for drug uses.

Questions about Herbalart Gida San Ve Tic Ltd

Is Herbalart Gida San Ve Tic Ltd on an FDA import alert?
Yes. As of October 26, 2026, Herbalart Gida San Ve Tic Ltd is on the red list of FDA Import Alert 54-16, “Foods/supplements with active pharmaceutical ingredient”, for stamina by honey- honey mixed herbal paste (aka epimedium mixed herbal paste); FDA published the listing on December 11, 2020.
Has FDA refused shipments from Herbalart Gida San Ve Tic Ltd?
Yes. FDA refused 2 shipment lines from Herbalart Gida San Ve Tic Ltd between March 30, 2020 and October 25, 2022. The most recent, on October 25, 2022, was vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c., charged as NO ENGLISH (required label information not in english).
Why did FDA refuse Herbalart Gida San Ve Tic Ltd's shipments?
The most frequent charges are LIST INGRE (ingredients not listed, 1 line) and NO ENGLISH (required label information not in english, 1 line).
What is Herbalart Gida San Ve Tic Ltd's FEI number?
Herbalart Gida San Ve Tic Ltd's FDA Establishment Identifier (FEI) is 3015909758.
Can shipments from Herbalart Gida San Ve Tic Ltd still enter the U.S.?
Shipments of stamina by honey- honey mixed herbal paste (aka epimedium mixed herbal paste) from Herbalart Gida San Ve Tic Ltd can be detained without physical examination under Import Alert 54-16; 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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Example subjectHerbalart Gida San Ve Tic Lt 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.