Ganesha Worldwide LLP
FDA import alert and refusal historyVadodara, IndiaFEI 3013884328
Recorded by FDA as GANESHA WORLDWIDE LLP
As of October 26, 2026, Ganesha Worldwide LLP (Vadodara, India) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for red mukhwas mouth freshener, published by FDA on November 27, 2017, and has 6 FDA import refusals recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 45-02 · red list
- Last import refusal
- Nuts or edible seeds not mentioned elsewhere, n.e.c. · COLOR LBLG
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Ganesha Worldwide LLP
7 records, newest first. Each line links to the FDA page it came from.
2025
- Import refusalRefused, Nuts or edible seeds not mentioned elsewhere, n.e.c.COLOR LBLGLACKS N/CNUTRIT LBLEntry 8GX-8010889-7Source
2023
- Import refusalRefused, Betel nut, nut flour/mealUNSAFE ADDPOISONORDEntry 8GX-8002762-6Source
2019
- Import refusalSource
Refused, 3 lines in one entry: Cardamon, ground, cracked (spice)UNSAFE COLEntry 9BM-0083640-6Show 3 linesHide lines
- Refused, Cardamon, ground, cracked (spice)UNSAFE COLEntry 9BM-0083640-6Source
- Refused, Cardamon, ground, cracked (spice)UNSAFE COLEntry 9BM-0083640-6Source
- Refused, Cardamon, ground, cracked (spice)UNSAFE COLEntry 9BM-0083640-6Source
2017
- Import refusalRefused, Cardamon, ground, cracked (spice)UNSAFE COLEntry 9BM-0060631-2Source
- Import alert listingListed on Import Alert 45-02red listRed Mukhwas Mouth FreshenerSource
Refusal charges, in plain English
- UNSAFE COL4 refused lines
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.
- COLOR LBLG1 refused line
Artificial coloring not declared
The product appeared to contain an artificial coloring without labeling that states that fact.
- LACKS N/C1 refused line
Net quantity statement missing
The packaged food appeared not to carry an accurate statement of the quantity of contents, such as net weight, measure, or count, on its label.
- NUTRIT LBL1 refused line
Nutrition information missing from label
The label or labeling appeared not to carry the nutrition information that U.S. law requires for the food.
- POISONORD1 refused line
Poisonous or deleterious substance (ordinarily injurious)
The product appeared to contain a poisonous or deleterious substance in a form or amount that would ordinarily render it injurious to health.
- UNSAFE ADD1 refused line
Food additive unsafe under section 409
The product appeared to contain a food additive that is unsafe within the meaning of section 409 of the FD&C Act, the section that governs which food additives may be used and under what conditions.
Questions about Ganesha Worldwide LLP
- Is Ganesha Worldwide LLP on an FDA import alert?
- Yes. As of October 26, 2026, Ganesha Worldwide LLP is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for red mukhwas mouth freshener; FDA published the listing on November 27, 2017.
- Has FDA refused shipments from Ganesha Worldwide LLP?
- Yes. FDA refused 6 shipment lines from Ganesha Worldwide LLP between December 1, 2017 and March 20, 2025. The most recent, on March 20, 2025, was nuts or edible seeds not mentioned elsewhere, n.e.c., charged as COLOR LBLG (artificial coloring not declared).
- Why did FDA refuse Ganesha Worldwide LLP's shipments?
- The most frequent charges are UNSAFE COL (color additive unsafe under section 721, 4 lines) and COLOR LBLG (artificial coloring not declared, 1 line).
- What is Ganesha Worldwide LLP's FEI number?
- Ganesha Worldwide LLP's FDA Establishment Identifier (FEI) is 3013884328.
- Can shipments from Ganesha Worldwide LLP still enter the U.S.?
- Shipments of red mukhwas mouth freshener from Ganesha Worldwide LLP can be detained without physical examination under Import Alert 45-02; 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.