Asia Exotic
FDA import alert and refusal historyPathumtani, ThailandFEI 3004280494
As of October 26, 2026, Asia Exotic (Pathumtani, Thailand) is on the red list of FDA Import Alert 99-05 (Raw agricultural products: pesticides) for durian; ginger; fresh, published by FDA on February 23, 2015, 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
- Durian, durion (subtropical and tropical fruit) · PESTICIDE
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Asia Exotic
2 records, newest first. Each line links to the FDA page it came from.
2019
2015
- Import alert listingListed on Import Alert 99-05red listDurian; Ginger; freshSource
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 Asia Exotic
- Is Asia Exotic on an FDA import alert?
- Yes. As of October 26, 2026, Asia Exotic is on the red list of FDA Import Alert 99-05, “Raw agricultural products: pesticides”, for durian; ginger; fresh; FDA published the listing on February 23, 2015.
- Has FDA refused shipments from Asia Exotic?
- Yes. FDA refused 1 shipment line from Asia Exotic on September 10, 2019. The most recent, on September 10, 2019, was durian, durion (subtropical and tropical fruit), charged as PESTICIDE (pesticide chemical residue).
- Why did FDA refuse Asia Exotic's shipments?
- The most frequent charge is PESTICIDE (pesticide chemical residue, 1 line).
- What is Asia Exotic's FEI number?
- Asia Exotic's FDA Establishment Identifier (FEI) is 3004280494.
- Can shipments from Asia Exotic still enter the U.S.?
- Shipments of durian; ginger; fresh from Asia Exotic 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.