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Productora y Comercializadora de Hortalizas Atardecer S de

FDA import alert and refusal historyPueblo Palmarito Tochapan, MexicoFEI 3010856171

Recorded by FDA as PRODUCTORA Y COMERCIALIZADORA DE HORTALIZAS ATARDECER S DE

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Example subjectProductora y Comercializadora de Hortalizas Atardecer S d added to Import Alert 16-129 (red list)

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As of October 26, 2026, Productora y Comercializadora de Hortalizas Atardecer S de (Pueblo Palmarito Tochapan, Mexico) is on the red list of FDA Import Alert 99-05 (Raw agricultural products: pesticides) for cilantro, published by FDA on December 5, 2022, is also listed on Import Alert 99-35 (red list), 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
Cilantro (leaf & stem vegetable) · PESTICIDE
Last warning letter
None found
Last inspection
None on record

Every FDA record for Productora y Comercializadora de Hortalizas Atardecer S de

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

2023

  1. Import refusal
    Refused, Cilantro (leaf & stem vegetable)PESTICIDEMFR INSANMFR INJEntry 9LN-2045262-9
    Source

2022

  1. Import refusal
    Refused, Cilantro (leaf & stem vegetable)PESTICIDEMFR INSANMFR INJEntry BJG-0137921-2
    Source
  2. Import alert listing
    Listed on Import Alert 99-05red listCilantro
    Source
  3. Import alert listing
    Listed on Import Alert 99-35red listCilantro
    Source

Refusal charges, in plain English

  • MFR INJ2 refused lines

    Insanitary conditions, may be injurious

    The product appeared to have been prepared, packed, or held under insanitary conditions whereby it may have been rendered injurious to health.

  • MFR INSAN2 refused lines

    Insanitary manufacturing, processing or packing

    The product appeared to have been manufactured, processed, or packed under insanitary conditions, which is a ground for refusal under section 801(a)(1) of the FD&C Act.

  • PESTICIDE2 refused lines

    Pesticide chemical residue

    The product appeared to contain a pesticide chemical residue that makes it adulterated under section 402(a)(2)(B) of the FD&C Act, for example a residue above the U.S. tolerance or one with no U.S. tolerance for that food.

Questions about Productora y Comercializadora de Hortalizas Atardecer S de

Is Productora y Comercializadora de Hortalizas Atardecer S de on an FDA import alert?
Yes. As of October 26, 2026, Productora y Comercializadora de Hortalizas Atardecer S de is on the red list of FDA Import Alert 99-05, “Raw agricultural products: pesticides”, for cilantro; FDA published the listing on December 5, 2022.
Has FDA refused shipments from Productora y Comercializadora de Hortalizas Atardecer S de?
Yes. FDA refused 2 shipment lines from Productora y Comercializadora de Hortalizas Atardecer S de between December 6, 2022 and November 16, 2023. The most recent, on November 16, 2023, was cilantro (leaf & stem vegetable), charged as PESTICIDE (pesticide chemical residue).
Why did FDA refuse Productora y Comercializadora de Hortalizas Atardecer S de's shipments?
The most frequent charges are MFR INJ (insanitary conditions, may be injurious, 2 lines) and MFR INSAN (insanitary manufacturing, processing or packing, 2 lines).
What is Productora y Comercializadora de Hortalizas Atardecer S de's FEI number?
Productora y Comercializadora de Hortalizas Atardecer S de's FDA Establishment Identifier (FEI) is 3010856171.
Can shipments from Productora y Comercializadora de Hortalizas Atardecer S de still enter the U.S.?
Shipments of cilantro from Productora y Comercializadora de Hortalizas Atardecer S de can be detained without physical examination under Import Alert 99-05; 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 subjectProductora y Comercializadora de Hortalizas Atardecer S d 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.