San Javier
FDA import alert and refusal historySantander, ColombiaFEI 3026960467
Recorded by FDA as SAN JAVIER
As of October 26, 2026, San Javier (Santander, Colombia) is on the red list of FDA Import Alert 99-05 (Raw agricultural products: pesticides) for limes, published by FDA on April 28, 2023, 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
- Lime (citrus) · PESTICIDE
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for San Javier
2 records, newest first. Each line links to the FDA page it came from.
2023
- Import alert listingListed on Import Alert 99-05red listLimesSource
- Import refusalRefused, Lime (citrus)PESTICIDEEntry 9P3-0282355-0Source
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 San Javier
- Is San Javier on an FDA import alert?
- Yes. As of October 26, 2026, San Javier is on the red list of FDA Import Alert 99-05, “Raw agricultural products: pesticides”, for limes; FDA published the listing on April 28, 2023.
- Has FDA refused shipments from San Javier?
- Yes. FDA refused 1 shipment line from San Javier on April 19, 2023. The most recent, on April 19, 2023, was lime (citrus), charged as PESTICIDE (pesticide chemical residue).
- Why did FDA refuse San Javier's shipments?
- The most frequent charge is PESTICIDE (pesticide chemical residue, 1 line).
- What is San Javier's FEI number?
- San Javier's FDA Establishment Identifier (FEI) is 3026960467.
- Can shipments from San Javier still enter the U.S.?
- Shipments of limes from San Javier 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.