Ricardo Machorro Avelino
FDA import alert and refusal historyLos Reyes De Juarez, MexicoFEI 3014065566
As of October 26, 2026, Ricardo Machorro Avelino (Los Reyes De Juarez, Mexico) is on the red list of FDA Import Alert 99-05 (Raw agricultural products: pesticides) for radishes, published by FDA on January 17, 2019, and has 4 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 Ricardo Machorro Avelino
5 records, newest first. Each line links to the FDA page it came from.
Refusal charges, in plain English
- PESTICIDE4 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 Ricardo Machorro Avelino
- Is Ricardo Machorro Avelino on an FDA import alert?
- Yes. As of October 26, 2026, Ricardo Machorro Avelino is on the red list of FDA Import Alert 99-05, “Raw agricultural products: pesticides”, for radishes; FDA published the listing on January 17, 2019.
- Has FDA refused shipments from Ricardo Machorro Avelino?
- Yes. FDA refused 4 shipment lines from Ricardo Machorro Avelino between October 18, 2018 and December 15, 2023. The most recent, on December 15, 2023, was radish (root & tuber vegetable), charged as PESTICIDE (pesticide chemical residue).
- Why did FDA refuse Ricardo Machorro Avelino's shipments?
- The most frequent charge is PESTICIDE (pesticide chemical residue, 4 lines).
- What is Ricardo Machorro Avelino's FEI number?
- Ricardo Machorro Avelino's FDA Establishment Identifier (FEI) is 3014065566.
- Can shipments from Ricardo Machorro Avelino still enter the U.S.?
- Shipments of radishes from Ricardo Machorro Avelino 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.