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Jose Benigno Osorio Oropeza

FDA import alert and refusal historyQuecholac, MexicoFEI 3028663338

Recorded by FDA as JOSE BENIGNO OSORIO OROPEZA

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Example subjectJose Benigno Osorio Oropez added to Import Alert 16-129 (red list)

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As of October 26, 2026, Jose Benigno Osorio Oropeza (Quecholac, Mexico) is on the red list of FDA Import Alert 99-05 (Raw agricultural products: pesticides) for chile de arbol (tree chili/pepper); chilaca pepper, published by FDA on December 19, 2025, and has 43 FDA import refusals recorded since October 2016.

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

Current status

Import alerts
IA 99-05 · red list
Last import refusal
Leaf & stem vegetables, n.e.c. · FSVP VIO
Last warning letter
None found
Last inspection
None on record

Every FDA record for Jose Benigno Osorio Oropeza

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

2026

  1. Import refusal
    Refused, 18 lines in one entry: Leaf & stem vegetables, n.e.c.; Prickle pear (core fruit) and 7 moreFSVP VIOEntry BYX-0311361-4Show 18 lines
    Source
  2. Import refusal
    Refused, 21 lines in one entry: Leaf & stem vegetables, n.e.c.; Prickle pear (core fruit) and 9 moreFSVP VIOEntry BYX-0310603-0Show 21 lines
    Source
  3. Import refusal
    Refused, Pepper, hot, n.e.c. (fruit used as vegetable)PESTICIDEEntry DR4-0692806-6
    Source
  4. Import refusal
    Refused, Pepper, hot, n.e.c. (fruit used as vegetable)PESTICIDEEntry 8MH-0110829-5
    Source

2025

  1. Import alert listing
    Listed on Import Alert 99-05red listCHILE DE ARBOL (Tree Chili/Pepper); Chilaca Pepper
    Source
  2. Import refusal
    Refused, 2 lines in one entry: Pepper, hot, n.e.c. (fruit used as vegetable)PESTICIDEEntry DR4-0671428-4Show 2 lines
    • Refused, Pepper, hot, n.e.c. (fruit used as vegetable)PESTICIDEEntry DR4-0671428-4Source
    • Refused, Pepper, hot, n.e.c. (fruit used as vegetable)PESTICIDEEntry DR4-0671428-4Source
    Source

Refusal charges, in plain English

  • FSVP VIO39 refused lines

    Importer not in compliance with FSVP

    The importer of record appeared not to be in compliance with the Foreign Supplier Verification Program requirements of section 805 of the FD&C Act. The charge concerns the importer's program, not a test result on the food.

  • PESTICIDE4 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 Jose Benigno Osorio Oropeza

Is Jose Benigno Osorio Oropeza on an FDA import alert?
Yes. As of October 26, 2026, Jose Benigno Osorio Oropeza is on the red list of FDA Import Alert 99-05, “Raw agricultural products: pesticides”, for chile de arbol (tree chili/pepper); chilaca pepper; FDA published the listing on December 19, 2025.
Has FDA refused shipments from Jose Benigno Osorio Oropeza?
Yes. FDA refused 43 shipment lines from Jose Benigno Osorio Oropeza between December 3, 2025 and July 2, 2026. The most recent, on July 2, 2026, was leaf & stem vegetables, n.e.c., charged as FSVP VIO (importer not in compliance with fsvp).
Why did FDA refuse Jose Benigno Osorio Oropeza's shipments?
The most frequent charges are FSVP VIO (importer not in compliance with fsvp, 39 lines) and PESTICIDE (pesticide chemical residue, 4 lines).
What is Jose Benigno Osorio Oropeza's FEI number?
Jose Benigno Osorio Oropeza's FDA Establishment Identifier (FEI) is 3028663338.
Can shipments from Jose Benigno Osorio Oropeza still enter the U.S.?
Shipments of chile de arbol (tree chili/pepper); chilaca pepper from Jose Benigno Osorio Oropeza 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 subjectJose Benigno Osorio Oropez 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.