Juventino Perez Jeronimo
FDA import alert and refusal historyTepeaca, MexicoFEI 3012312523
As of October 26, 2026, Juventino Perez Jeronimo (Tepeaca, Mexico) is on the red list of FDA Import Alert 99-05 (Raw agricultural products: pesticides) for radish, published by FDA on March 3, 2022, 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
- White radish (root & tuber vegetable) · PESTICIDE
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Juventino Perez Jeronimo
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 Juventino Perez Jeronimo
- Is Juventino Perez Jeronimo on an FDA import alert?
- Yes. As of October 26, 2026, Juventino Perez Jeronimo is on the red list of FDA Import Alert 99-05, “Raw agricultural products: pesticides”, for radish; FDA published the listing on March 3, 2022.
- Has FDA refused shipments from Juventino Perez Jeronimo?
- Yes. FDA refused 2 shipment lines from Juventino Perez Jeronimo between February 23, 2022 and April 26, 2022. The most recent, on April 26, 2022, was white radish (root & tuber vegetable), charged as PESTICIDE (pesticide chemical residue).
- Why did FDA refuse Juventino Perez Jeronimo's shipments?
- The most frequent charge is PESTICIDE (pesticide chemical residue, 2 lines).
- What is Juventino Perez Jeronimo's FEI number?
- Juventino Perez Jeronimo's FDA Establishment Identifier (FEI) is 3012312523.
- Can shipments from Juventino Perez Jeronimo still enter the U.S.?
- Shipments of radish from Juventino Perez Jeronimo 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.