Agricola San Pedro
FDA import alert and refusal historyLeon, MexicoFEI 3010805582
As of October 26, 2026, Agricola San Pedro (Leon, Mexico) is on the red list of FDA Import Alert 99-05 (Raw agricultural products: pesticides) for fresh celery, published by FDA on February 10, 2017, and has 1 FDA import refusal 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
- Celery (leaf & stem vegetable) · PESTICIDE
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Agricola San Pedro
2 records, newest first. Each line links to the FDA page it came from.
2017
- Import alert listingListed on Import Alert 99-05red listFresh CelerySource
2016
Refusal charges, in plain English
- PESTICIDE1 refused line
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 San Pedro
- Is Agricola San Pedro on an FDA import alert?
- Yes. As of October 26, 2026, Agricola San Pedro is on the red list of FDA Import Alert 99-05, “Raw agricultural products: pesticides”, for fresh celery; FDA published the listing on February 10, 2017.
- Has FDA refused shipments from Agricola San Pedro?
- Yes. FDA refused 1 shipment line from Agricola San Pedro on December 21, 2016. The most recent, on December 21, 2016, was celery (leaf & stem vegetable), charged as PESTICIDE (pesticide chemical residue).
- Why did FDA refuse Agricola San Pedro's shipments?
- The most frequent charge is PESTICIDE (pesticide chemical residue, 1 line).
- What is Agricola San Pedro's FEI number?
- Agricola San Pedro's FDA Establishment Identifier (FEI) is 3010805582.
- Can shipments from Agricola San Pedro still enter the U.S.?
- Shipments of fresh celery from Agricola San Pedro 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.