Udaan International
FDA import alert and refusal historyAhmedabad, IndiaFEI 3012318734
As of October 25, 2026, Udaan International (Ahmedabad, India) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for tuttyfruity "tooty fruity", published by FDA on January 11, 2018, and has 5 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
- Beverage base of non-fruit origin, n.e.c. · LACKS FIRM
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Udaan International
6 records, newest first. Each line links to the FDA page it came from.
2020
- Import refusalRefused, Beverage base of non-fruit origin, n.e.c.LACKS FIRMNUTRIT LBLEntry H67-1590613-6Source
2018
- Import refusalRefused, Gelatin, n.e.c.UNSAFE COLLIST INGREPRESRV LBLLABELINGNUTRIT LBLYELLOW #5Entry B7P-0000506-2Source
- Import alert listingListed on Import Alert 45-02red listTuttyfruity "Tooty Fruity"Source
2017
- Import refusalSource
Refused, 3 lines in one entry: Other bakery products, n.e.c.FILTHYEntry B7P-0000331-5Show 3 linesHide lines
Refusal charges, in plain English
- FILTHY3 refused lines
Filthy, putrid or decomposed substance
The product appeared to consist in whole or in part of a filthy, putrid, or decomposed substance, or to be otherwise unfit for food.
- NUTRIT LBL2 refused lines
Nutrition information missing from label
The label or labeling appeared not to carry the nutrition information that U.S. law requires for the food.
- LABELING1 refused line
Fair Packaging and Labeling Act
The package appeared not to meet the Fair Packaging and Labeling Act because of the placement, form, or contents of a required label statement.
- LACKS FIRM1 refused line
Manufacturer name and address missing
The packaged product's label appeared not to show the name and place of business of the manufacturer, packer, or distributor.
- LIST INGRE1 refused line
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).
- PRESRV LBL1 refused line
Chemical preservative not declared
The product appeared to contain a chemical preservative without labeling that states that fact and the preservative's function.
- 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.
- YELLOW #51 refused line
FD&C Yellow No. 5 not declared
The food appeared to contain the color additive FD&C Yellow No. 5 without declaring it on the label as 21 CFR 74.705 requires.
Questions about Udaan International
- Is Udaan International on an FDA import alert?
- Yes. As of October 25, 2026, Udaan International is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for tuttyfruity "tooty fruity"; FDA published the listing on January 11, 2018.
- Has FDA refused shipments from Udaan International?
- Yes. FDA refused 5 shipment lines from Udaan International between July 12, 2017 and November 30, 2020. The most recent, on November 30, 2020, was beverage base of non-fruit origin, n.e.c., charged as LACKS FIRM (manufacturer name and address missing).
- Why did FDA refuse Udaan International's shipments?
- The most frequent charges are FILTHY (filthy, putrid or decomposed substance, 3 lines) and NUTRIT LBL (nutrition information missing from label, 2 lines).
- What is Udaan International's FEI number?
- Udaan International's FDA Establishment Identifier (FEI) is 3012318734.
- Can shipments from Udaan International still enter the U.S.?
- Shipments of tuttyfruity "tooty fruity" from Udaan International 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.