Kanha Enterprises
FDA import alert and refusal historyIndore, IndiaFEI 3011172207
As of October 26, 2026, Kanha Enterprises (Indore, India) is on the red list of FDA Import Alert 99-08 (Processed human and animal foods: pesticides) for basmati rice, published by FDA on January 11, 2019, and has 3 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, plain (white or polished) processed (packaged) · PESTICIDE
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Kanha Enterprises
4 records, newest first. Each line links to the FDA page it came from.
2020
2019
Refusal charges, in plain English
- PESTICIDE3 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 Kanha Enterprises
- Is Kanha Enterprises on an FDA import alert?
- Yes. As of October 26, 2026, Kanha Enterprises 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 January 11, 2019.
- Has FDA refused shipments from Kanha Enterprises?
- Yes. FDA refused 3 shipment lines from Kanha Enterprises between January 17, 2019 and February 28, 2020. The most recent, on February 28, 2020, was rice, plain (white or polished) processed (packaged), charged as PESTICIDE (pesticide chemical residue).
- Why did FDA refuse Kanha Enterprises's shipments?
- The most frequent charge is PESTICIDE (pesticide chemical residue, 3 lines).
- What is Kanha Enterprises's FEI number?
- Kanha Enterprises's FDA Establishment Identifier (FEI) is 3011172207.
- Can shipments from Kanha Enterprises still enter the U.S.?
- Shipments of basmati rice from Kanha Enterprises 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.