Josue Frausto Montoya
FDA import alert and refusal historyLoreto, MexicoFEI 3017093574
As of October 26, 2026, Josue Frausto Montoya (Loreto, Mexico) is on the red list of FDA Import Alert 99-05 (Raw agricultural products: pesticides) for lettuce, published by FDA on July 23, 2024, and has 3 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
- Lettuce, head (e.g. iceberg) (leaf & stem vegetable) · PESTICIDE
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Josue Frausto Montoya
4 records, newest first. Each line links to the FDA page it came from.
2026
2024
Refusal charges, in plain English
- PESTICIDE3 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 Josue Frausto Montoya
- Is Josue Frausto Montoya on an FDA import alert?
- Yes. As of October 26, 2026, Josue Frausto Montoya is on the red list of FDA Import Alert 99-05, “Raw agricultural products: pesticides”, for lettuce; FDA published the listing on July 23, 2024.
- Has FDA refused shipments from Josue Frausto Montoya?
- Yes. FDA refused 3 shipment lines from Josue Frausto Montoya between June 27, 2024 and March 5, 2026. The most recent, on March 5, 2026, was lettuce, head (e.g. iceberg) (leaf & stem vegetable), charged as PESTICIDE (pesticide chemical residue).
- Why did FDA refuse Josue Frausto Montoya's shipments?
- The most frequent charge is PESTICIDE (pesticide chemical residue, 3 lines).
- What is Josue Frausto Montoya's FEI number?
- Josue Frausto Montoya's FDA Establishment Identifier (FEI) is 3017093574.
- Can shipments from Josue Frausto Montoya still enter the U.S.?
- Shipments of lettuce from Josue Frausto Montoya 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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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.