Natvar & Company
FDA import alert and refusal historyDubai, United Arab EmiratesFEI 1000606211
As of October 26, 2026, Natvar & Company (Dubai, United Arab Emirates) is on the red list of FDA Import Alert 99-08 (Processed human and animal foods: pesticides) for basmati rice, published by FDA on August 12, 2025, 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 99-08 · red list
- Last import refusal
- Rice, basmati, processed (packaged) · PESTICIDE
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Natvar & Company
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 Natvar & Company
- Is Natvar & Company on an FDA import alert?
- Yes. As of October 26, 2026, Natvar & Company is on the red list of FDA Import Alert 99-08, “Processed human and animal foods: pesticides”, for basmati rice; FDA published the listing on August 12, 2025.
- Has FDA refused shipments from Natvar & Company?
- Yes. FDA refused 2 shipment lines from Natvar & Company between August 28, 2025 and October 17, 2025. The most recent, on October 17, 2025, was rice, basmati, processed (packaged), charged as PESTICIDE (pesticide chemical residue).
- Why did FDA refuse Natvar & Company's shipments?
- The most frequent charge is PESTICIDE (pesticide chemical residue, 2 lines).
- What is Natvar & Company's FEI number?
- Natvar & Company's FDA Establishment Identifier (FEI) is 1000606211.
- Can shipments from Natvar & Company still enter the U.S.?
- Shipments of basmati rice from Natvar & Company can be detained without physical examination under Import Alert 99-08; 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.