Kitchen Xpress Overseas Limited
FDA import alert and refusal historyGandhidham, IndiaFEI 3009070354
Recorded by FDA as KITCHEN XPRESS OVERSEAS LIMITED
As of October 26, 2026, Kitchen Xpress Overseas Limited (GANDHIDHAM, India) is on the red list of FDA Import Alert 99-08 (Processed human and animal foods: pesticides) for urad dal; masoor dal (split red lentils), published by FDA on July 18, 2022, and has 13 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
- Bean, corn, pea, dried or paste, n.e.c. (vegetable) · PESTICIDE
- Last warning letter
- None found
- Last inspection
- Classified NAI (No Action Indicated)
Every FDA record for Kitchen Xpress Overseas Limited
15 records, newest first. Each line links to the FDA page it came from.
2024
- Import refusalSource
Refused, 2 lines in one entry: Bean, corn, pea, dried or paste, n.e.c. (vegetable)PESTICIDEEntry KM6-3631251-4Show 2 linesHide lines
2023
2022
- Import refusalRefused, Lentils, dried or pastePESTICIDEEntry KM6-3581895-8Source
- Import refusalSource
Refused, 2 lines in one entry: Lentils, dried or pastePESTICIDEEntry KM6-3581511-1Show 2 linesHide lines
- Import refusalSource
Refused, 2 lines in one entry: Lentils, dried or pastePESTICIDEPOISONOUSEntry KM6-3577469-8Show 2 linesHide lines
- Import refusalRefused, Lentils, dried or pastePESTICIDEEntry KM6-3581120-1Source
- Import refusalSource
Refused, 2 lines in one entry: Lentils, dried or pastePESTICIDEEntry KM6-3580073-3Show 2 linesHide lines
- Import alert listingListed on Import Alert 99-08red listUrad dal; masoor dal (split red lentils)Source
2019
- Import refusalRefused, Garbanzo beanSALMONELLAEntry B9G-0009313-0Source
2017
- InspectionInspection classified NAI (No Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological HazardsSource
Refusal charges, in plain English
- PESTICIDE11 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.
- 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.
- SALMONELLA1 refused line
Salmonella
The product appeared to contain Salmonella, which the law treats as a poisonous and deleterious substance that may make food injurious to health.
Questions about Kitchen Xpress Overseas Limited
- Is Kitchen Xpress Overseas Limited on an FDA import alert?
- Yes. As of October 26, 2026, Kitchen Xpress Overseas Limited is on the red list of FDA Import Alert 99-08, “Processed human and animal foods: pesticides”, for urad dal; masoor dal (split red lentils); FDA published the listing on July 18, 2022.
- Has FDA refused shipments from Kitchen Xpress Overseas Limited?
- Yes. FDA refused 13 shipment lines from Kitchen Xpress Overseas Limited between June 25, 2019 and September 11, 2024. The most recent, on September 11, 2024, was bean, corn, pea, dried or paste, n.e.c. (vegetable), charged as PESTICIDE (pesticide chemical residue).
- Why did FDA refuse Kitchen Xpress Overseas Limited's shipments?
- The most frequent charges are PESTICIDE (pesticide chemical residue, 11 lines) and POISONOUS (poisonous or deleterious substance, 1 line).
- When was Kitchen Xpress Overseas Limited last inspected by FDA?
- FDA's most recent inspection of Kitchen Xpress Overseas Limited with a final classification is dated June 6, 2017 and was classified NAI (No Action Indicated).
- What is Kitchen Xpress Overseas Limited's FEI number?
- Kitchen Xpress Overseas Limited's FDA Establishment Identifier (FEI) is 3009070354.
- Can shipments from Kitchen Xpress Overseas Limited still enter the U.S.?
- Shipments of urad dal; masoor dal (split red lentils) from Kitchen Xpress Overseas Limited 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.