D.A. Patel
FDA import alert and refusal historyUnjha, IndiaFEI 3009992663
As of October 26, 2026, D.A. Patel (Unjha, India) is on the red list of FDA Import Alert 99-08 (Processed human and animal foods: pesticides) for sortex natural sesame seed, published by FDA on January 6, 2025, is also listed on Import Alert 99-42 (red list) and Import Alert 45-02 (red list), and has 6 FDA import refusals recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Last import refusal
- Sesame seed (edible seed) · PESTICIDE
- Last warning letter
- None found
- Last inspection
- Classified NAI (No Action Indicated)
Every FDA record for D.A. Patel
10 records, newest first. Each line links to the FDA page it came from.
2025
- Import refusalRefused, Sesame seed (edible seed)PESTICIDEEntry KM6-1622557-9Source
- Import alert listingListed on Import Alert 99-08red listSortex natural sesame seedSource
2024
- Import refusalRefused, Cinnamon, cassia, ground, cracked (spice)POISONOUSEntry 316-2070388-9Source
- Import alert listingListed on Import Alert 99-42red listCinnamon powderSource
- Import alert listingListed on Import Alert 45-02red listCandy Coated Fennel Seeds (Candy Souff)Source
2022
- Import refusalRefused, Fennel, whole (spice)UNSAFE COLCOLOR LBLGEntry KM6-1567046-0Source
2019
- Import refusalSource
Refused, 3 lines in one entry: Fennel, whole (spice)LIST INGRECOLOR LBLGEntry 316-2030570-1Show 3 linesHide lines
- Refused, Fennel, whole (spice)LIST INGRECOLOR LBLGEntry 316-2030570-1Source
- Refused, Fennel, whole (spice)LIST INGRECOLOR LBLGEntry 316-2030570-1Source
- Refused, Fennel, whole (spice)LIST INGRECOLOR LBLGEntry 316-2030570-1Source
2018
- InspectionInspection classified NAI (No Action Indicated)Foodborne Biological HazardsSource
Refusal charges, in plain English
- COLOR LBLG4 refused lines
Artificial coloring not declared
The product appeared to contain an artificial coloring without labeling that states that fact.
- LIST INGRE3 refused lines
Ingredients not listed
The product is made from two or more ingredients and the label appeared not to list the common or usual name of each one (or, for a juice beverage, the percentage of juice).
- 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.
- POISONOUS1 refused line
Poisonous or deleterious substance
The product appeared to bear or contain a poisonous or deleterious substance which may render it injurious to health.
- UNSAFE COL1 refused line
Color additive unsafe under section 721
The product appeared to be, or to contain, a color additive that is unsafe within the meaning of section 721(a) of the FD&C Act, the section that governs which color additives may be used and how.
Questions about D.A. Patel
- Is D.A. Patel on an FDA import alert?
- Yes. As of October 26, 2026, D.A. Patel is on the red list of FDA Import Alert 99-08, “Processed human and animal foods: pesticides”, for sortex natural sesame seed; FDA published the listing on January 6, 2025.
- Has FDA refused shipments from D.A. Patel?
- Yes. FDA refused 6 shipment lines from D.A. Patel between February 11, 2019 and January 28, 2025. The most recent, on January 28, 2025, was sesame seed (edible seed), charged as PESTICIDE (pesticide chemical residue).
- Why did FDA refuse D.A. Patel's shipments?
- The most frequent charges are COLOR LBLG (artificial coloring not declared, 4 lines) and LIST INGRE (ingredients not listed, 3 lines).
- When was D.A. Patel last inspected by FDA?
- FDA's most recent inspection of D.A. Patel with a final classification is dated August 31, 2018 and was classified NAI (No Action Indicated).
- What is D.A. Patel's FEI number?
- D.A. Patel's FDA Establishment Identifier (FEI) is 3009992663.
- Can shipments from D.A. Patel still enter the U.S.?
- Shipments of sortex natural sesame seed from D.A. Patel 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.