Arrayanes
FDA import alert and refusal historyBogota, ColombiaFEI 3025539508
Recorded by FDA as ARRAYANES
As of October 25, 2026, Arrayanes (Bogota, Colombia) is on the red list of FDA Import Alert 99-05 (Raw agricultural products: pesticides) for limes, published by FDA on March 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 Arrayanes
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 9P3-0271388-4Source
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 Arrayanes
- Is Arrayanes on an FDA import alert?
- Yes. As of October 25, 2026, Arrayanes is on the red list of FDA Import Alert 99-05, “Raw agricultural products: pesticides”, for limes; FDA published the listing on March 28, 2023.
- Has FDA refused shipments from Arrayanes?
- Yes. FDA refused 1 shipment line from Arrayanes on February 10, 2023. The most recent, on February 10, 2023, was lime (citrus), charged as PESTICIDE (pesticide chemical residue).
- Why did FDA refuse Arrayanes's shipments?
- The most frequent charge is PESTICIDE (pesticide chemical residue, 1 line).
- What is Arrayanes's FEI number?
- Arrayanes's FDA Establishment Identifier (FEI) is 3025539508.
- Can shipments from Arrayanes still enter the U.S.?
- Shipments of limes from Arrayanes 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.