Agricola Valencia
FDA import alert and refusal historyGuaymas, MexicoFEI 3015898096
Recorded by FDA as AGRICOLA VALENCIA
As of October 26, 2026, Agricola Valencia (Guaymas, Mexico) is on the red list of FDA Import Alert 99-05 (Raw agricultural products: pesticides) for jalapeno pepper, published by FDA on February 22, 2023, 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
- Jalapeno pepper, hot (fruit used as vegetable) · PESTICIDE
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Agricola Valencia
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 Agricola Valencia
- Is Agricola Valencia on an FDA import alert?
- Yes. As of October 26, 2026, Agricola Valencia is on the red list of FDA Import Alert 99-05, “Raw agricultural products: pesticides”, for jalapeno pepper; FDA published the listing on February 22, 2023.
- Has FDA refused shipments from Agricola Valencia?
- Yes. FDA refused 2 shipment lines from Agricola Valencia between February 9, 2023 and January 24, 2025. The most recent, on January 24, 2025, was jalapeno pepper, hot (fruit used as vegetable), charged as PESTICIDE (pesticide chemical residue).
- Why did FDA refuse Agricola Valencia's shipments?
- The most frequent charge is PESTICIDE (pesticide chemical residue, 2 lines).
- What is Agricola Valencia's FEI number?
- Agricola Valencia's FDA Establishment Identifier (FEI) is 3015898096.
- Can shipments from Agricola Valencia still enter the U.S.?
- Shipments of jalapeno pepper from Agricola Valencia 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.