Mehrotra Consumer Products Private Limited
⚠️ High Risk
FEI: 3011002690 • Greater Noida, Uttar Pradesh • INDIA
FEI Number
3011002690
Location
Greater Noida, Uttar Pradesh
Country
INDIAAddress
Ecotech 1, 26g Sector 31, Greater Noida, Uttar Pradesh, India
High Risk
FDA Import Risk Assessment
This firm has a significant history of FDA import refusals with notable violations.
Statistics
Score Breakdown
How is this score calculated?
Proprietary Algorithm
- 40% Violation Severity — AI-assessed (1-10)
- 30% Refusal Volume — Logarithmic scale
- 20% Recency — Decays over 5 years
- 10% Frequency — Refusals per year
© ImportRefusal.com Original Analysis
Violation Summary
UNSAFE ADD
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain an unsafe food additive within the meaning of section 409.
FILTHY
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the article appears to consist in whole or in part of a filthy, putrid, or decomposed substance or be otherwise unfit for food.
AFLATOXIN
The article appears to contain a mycotoxin, a poisonous and deleterious substance which may render it injurious to health.
LACKS N/C
The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(e)(2) of the FD&C Act in that the food is in package form and the label fails to bear an accurate statement of the quantity of the contents in terms of weight, measure, or numerical count in accordance with Section 403(e)(2) of the FD&C Act.
USUAL NAME
The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(i)(1) of the FD&C Act in that the label fails to bear the common or usual name of the food, if any there be.
LABELING
The article appears in violation of FPLA because of its placement, form and/or contents statement.
HEALTH C
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be misbranded in that the label or labeling bears an unauthorized nutrient content/health claim.
DIRECTIONS
The article is subject to refusal of admission pursuant to section 801(a)(3) in that it is a device whose label appears to not bear adequate directions for use.
UNAPPROVED
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a new drug within the meaning of Section 201(p) without an approved New Drug Application (NDA).
LIST INGRE
The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(i)(2) of the FD&C Act in that it is fabricated from two or more ingredients and the label fails to bear the common or usual name of each such ingredient and/or the article purports to be a beverage containing vegetable or fruit juice, but does not bear a statement with appropriate prominence on the information panel of the total percentage of such fruit or vegetable juice contained in the food.
INCONSPICU
The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(f) of the FD&C Act in that any word, statement, or other information required by or under the authority of the FD&C Act to appear on the label or labeling is not prominently placed thereon with such conspicuousness (as compared with other words, statements, designs, or devices, in the labeling) and in such terms as to render it likely to be read and understood by the ordinary individual under customary terms of purchase and use (for example, label contains information in two or more languages but fails to repeat all required information in both languages in accordance with 21 CFR 101.15(c)(2), or label fails to include all required information in English in accordance with 21 CFR 101.15(c)(1), except in the case of articles distributed solely in the Commonwealth of Puerto Rico or in a Territory where the predominant language is one other than English)).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 10/9/2025 | 26AYY12MUSTARD OIL, CRUDE, SEE 28O FOR MUSTARD OIL AS A FLAVORING | 238UNSAFE ADD | Division of Northeast Imports (DNEI) |
| 10/9/2025 | 26AYY12MUSTARD OIL, CRUDE, SEE 28O FOR MUSTARD OIL AS A FLAVORING | 238UNSAFE ADD | Division of Northeast Imports (DNEI) |
| 10/9/2025 | 26AYY12MUSTARD OIL, CRUDE, SEE 28O FOR MUSTARD OIL AS A FLAVORING | 238UNSAFE ADD | Division of Northeast Imports (DNEI) |
| 4/18/2023 | 26CHN11MUSTARD OIL, REFINED, SINGLE INGREDIENT, SEE 28O FOR MUSTARD OIL AS A FLAVORING | 238UNSAFE ADD | Division of West Coast Imports (DWCI) |
| 4/18/2023 | 26CHN11MUSTARD OIL, REFINED, SINGLE INGREDIENT, SEE 28O FOR MUSTARD OIL AS A FLAVORING | 238UNSAFE ADD | Division of West Coast Imports (DWCI) |
| 4/6/2023 | 26CHN11MUSTARD OIL, REFINED, SINGLE INGREDIENT, SEE 28O FOR MUSTARD OIL AS A FLAVORING | 238UNSAFE ADD | Division of Northeast Imports (DNEI) |
| 3/26/2019 | 25YFT99VEGETABLE & VEGETABLE PRODUCTS NOT MENTIONED ELSEWHERE, N.E.C. | Division of West Coast Imports (DWCI) | |
| 8/31/2018 | 02BGT01CORN, BOLTED MEAL OR FLOUR | 297AFLATOXIN | Division of Southwest Imports (DSWI) |
| 8/3/2017 | 21TGH14TAMARIND, DRIED OR PASTE | 249FILTHY | Division of Southwest Imports (DSWI) |
| 7/20/2017 | 02BGT01CORN, BOLTED MEAL OR FLOUR | 297AFLATOXIN | Division of Southwest Imports (DSWI) |
| 10/23/2014 | 02DGT07RICE, BASMATI, PROCESSED (PACKAGED) | 249FILTHY | Seattle District Office (SEA-DO) |
| 10/23/2014 | 02DGT07RICE, BASMATI, PROCESSED (PACKAGED) | 249FILTHY | Seattle District Office (SEA-DO) |
Frequently Asked Questions
What is Mehrotra Consumer Products Private Limited's FDA import refusal history?
Mehrotra Consumer Products Private Limited (FEI: 3011002690) has 12 FDA import refusal record(s) in our database, spanning from 10/23/2014 to 10/9/2025.
What is an FEI number?
FEI stands for Firm Establishment Identifier. It's a unique number assigned by the FDA to identify establishments that manufacture, process, pack, or hold food, drugs, medical devices, or other FDA-regulated products. Mehrotra Consumer Products Private Limited's FEI number is 3011002690.
What types of violations has Mehrotra Consumer Products Private Limited received?
Mehrotra Consumer Products Private Limited has been cited for 11 different violation type(s). Common FDA violations include adulteration (unsafe or unsanitary products), misbranding (incorrect or misleading labels), and regulatory non-compliance.
Where does this information about Mehrotra Consumer Products Private Limited come from?
All FDA import refusal data for Mehrotra Consumer Products Private Limited is sourced from the official FDA Data Dashboard (datadashboard.fda.gov), a public government database maintained by the U.S. Food and Drug Administration.
Data sourced from the FDA Data Dashboard, a public database maintained by the U.S. Food and Drug Administration.