Martin Lozano Rosas
FDA import alert and refusal historyQuecholac, MexicoFEI 3029648154
Recorded by FDA as MARTIN LOZANO ROSAS
As of October 26, 2026, Martin Lozano Rosas (Quecholac, Mexico) is on the red list of FDA Import Alert 99-05 (Raw agricultural products: pesticides) for radish, published by FDA on July 2, 2024, and has 2 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
- Radish (root & tuber vegetable) · PESTICIDE
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Martin Lozano Rosas
3 records, newest first. Each line links to the FDA page it came from.
Refusal charges, in plain English
- 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 Martin Lozano Rosas
- Is Martin Lozano Rosas on an FDA import alert?
- Yes. As of October 26, 2026, Martin Lozano Rosas is on the red list of FDA Import Alert 99-05, “Raw agricultural products: pesticides”, for radish; FDA published the listing on July 2, 2024.
- Has FDA refused shipments from Martin Lozano Rosas?
- Yes. FDA refused 2 shipment lines from Martin Lozano Rosas between February 26, 2024 and March 13, 2024. The most recent, on March 13, 2024, was radish (root & tuber vegetable), charged as PESTICIDE (pesticide chemical residue).
- Why did FDA refuse Martin Lozano Rosas's shipments?
- The most frequent charge is PESTICIDE (pesticide chemical residue, 2 lines).
- What is Martin Lozano Rosas's FEI number?
- Martin Lozano Rosas's FDA Establishment Identifier (FEI) is 3029648154.
- Can shipments from Martin Lozano Rosas still enter the U.S.?
- Shipments of radish from Martin Lozano Rosas 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.