Ruben Miron Miron
FDA import alert and refusal historyQuecholac, MexicoFEI 3014999250
Recorded by FDA as RUBEN MIRON MIRON
As of October 26, 2026, Ruben Miron Miron (Quecholac, Mexico) is on the red list of FDA Import Alert 99-05 (Raw agricultural products: pesticides) for cilantro, published by FDA on January 2, 2025, 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
- Cilantro (leaf & stem vegetable) · PESTICIDE
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Ruben Miron 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 Ruben Miron Miron
- Is Ruben Miron Miron on an FDA import alert?
- Yes. As of October 26, 2026, Ruben Miron Miron is on the red list of FDA Import Alert 99-05, “Raw agricultural products: pesticides”, for cilantro; FDA published the listing on January 2, 2025.
- Has FDA refused shipments from Ruben Miron Miron?
- Yes. FDA refused 2 shipment lines from Ruben Miron Miron between December 13, 2024 and December 27, 2024. The most recent, on December 27, 2024, was cilantro (leaf & stem vegetable), charged as PESTICIDE (pesticide chemical residue).
- Why did FDA refuse Ruben Miron Miron's shipments?
- The most frequent charge is PESTICIDE (pesticide chemical residue, 2 lines).
- What is Ruben Miron Miron's FEI number?
- Ruben Miron Miron's FDA Establishment Identifier (FEI) is 3014999250.
- Can shipments from Ruben Miron Miron still enter the U.S.?
- Shipments of cilantro from Ruben Miron 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.