Rafael Duarte Miron
FDA import alert and refusal historyEnsenada, MexicoFEI 3030982079
Recorded by FDA as RAFAEL DUARTE MIRON
As of October 26, 2026, Rafael Duarte Miron (Ensenada, Mexico) is on the red list of FDA Import Alert 99-05 (Raw agricultural products: pesticides) for green onions, published by FDA on August 29, 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
- Scallions, green onions (root & tuber vegetable) · PESTICIDE
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Rafael Duarte Miron
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 Rafael Duarte Miron
- Is Rafael Duarte Miron on an FDA import alert?
- Yes. As of October 26, 2026, Rafael Duarte Miron is on the red list of FDA Import Alert 99-05, “Raw agricultural products: pesticides”, for green onions; FDA published the listing on August 29, 2024.
- Has FDA refused shipments from Rafael Duarte Miron?
- Yes. FDA refused 2 shipment lines from Rafael Duarte Miron between August 13, 2024 and January 23, 2025. The most recent, on January 23, 2025, was scallions, green onions (root & tuber vegetable), charged as PESTICIDE (pesticide chemical residue).
- Why did FDA refuse Rafael Duarte Miron's shipments?
- The most frequent charge is PESTICIDE (pesticide chemical residue, 2 lines).
- What is Rafael Duarte Miron's FEI number?
- Rafael Duarte Miron's FDA Establishment Identifier (FEI) is 3030982079.
- Can shipments from Rafael Duarte Miron still enter the U.S.?
- Shipments of green onions from Rafael Duarte Miron 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.