SupplierRadar

Industrial de Oleaginosas SA de CV

FDA import alert and refusal historyGuadalajara, MexicoFEI 3003584338

Recorded by FDA as INDUSTRIAL DE OLEAGINOSAS SA DE CV

Watch this supplier

Watch this supplier

Get an email when FDA publishes anything new on Industrial de Oleaginosas SA de CV.

Enter your work email and confirm with the link we send. Your first supplier is free, with no password and no card.

Example subjectIndustrial de Oleaginosas SA de C added to Import Alert 16-129 (red list)

Free for one supplier. No password, no card.

As of October 26, 2026, Industrial de Oleaginosas SA de CV (Guadalajara, Mexico) is on the red list of FDA Import Alert 99-19 (Food products: Salmonella) for soybean flour meal; or powder (textured soy protein), published by FDA on March 2, 2016, and has 5 FDA import refusals recorded since October 2016.

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

Current status

Last import refusal
Soybeans (see industry 37 for bean curd), dried or paste · SALMONELLA
Last warning letter
None found
Last inspection
None on record

Every FDA record for Industrial de Oleaginosas SA de CV

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

2025

  1. Import refusal
    Refused, Soybeans (see industry 37 for bean curd), dried or pasteSALMONELLAEntry BJG-0184987-5
    Source

2023

  1. Import refusal
    Refused, Soybean flour, meal, or powderSALMONELLAEntry BJG-0153074-9
    Source

2017

  1. Import refusal
    Refused, Soybean flour, meal, or powderSALMONELLAEntry 9QW-1171069-4
    Source
  2. Import refusal
    Refused, Soybean flour, meal, or powderSALMONELLAEntry 9QW-1167520-2
    Source

2016

  1. Import refusal
    Refused, Soybean flour, meal, or powderSALMONELLAEntry H87-0221289-0
    Source
  2. Import alert listing
    Listed on Import Alert 99-19red listSoybean Flour Meal; or Powder (Textured Soy Protein)
    Source

Refusal charges, in plain English

  • SALMONELLA5 refused lines

    Salmonella

    The product appeared to contain Salmonella, which the law treats as a poisonous and deleterious substance that may make food injurious to health.

Questions about Industrial de Oleaginosas SA de CV

Is Industrial de Oleaginosas SA de CV on an FDA import alert?
Yes. As of October 26, 2026, Industrial de Oleaginosas SA de CV is on the red list of FDA Import Alert 99-19, “Food products: Salmonella”, for soybean flour meal; or powder (textured soy protein); FDA published the listing on March 2, 2016.
Has FDA refused shipments from Industrial de Oleaginosas SA de CV?
Yes. FDA refused 5 shipment lines from Industrial de Oleaginosas SA de CV between October 24, 2016 and January 7, 2025. The most recent, on January 7, 2025, was soybeans (see industry 37 for bean curd), dried or paste, charged as SALMONELLA (salmonella).
Why did FDA refuse Industrial de Oleaginosas SA de CV's shipments?
The most frequent charge is SALMONELLA (salmonella, 5 lines).
What is Industrial de Oleaginosas SA de CV's FEI number?
Industrial de Oleaginosas SA de CV's FDA Establishment Identifier (FEI) is 3003584338.
Can shipments from Industrial de Oleaginosas SA de CV still enter the U.S.?
Shipments of soybean flour meal; or powder (textured soy protein) from Industrial de Oleaginosas SA de CV can be detained without physical examination under Import Alert 99-19; 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).

Buying from Industrial de Oleaginosas SA de CV?

Watch it and get the FDA record the day it changes. Free for one supplier.

Watch this supplier

Watch this supplier

Get an email when FDA publishes anything new on Industrial de Oleaginosas SA de CV.

Enter your work email and confirm with the link we send. Your first supplier is free, with no password and no card.

Example subjectIndustrial de Oleaginosas SA de C added to Import Alert 16-129 (red list)

Free for one supplier. No password, no card.

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.