H.K. Exports
FDA import alert and refusal historyAhmedabad, IndiaFEI 3010326532
Recorded by FDA as H.K. EXPORTS
As of October 26, 2026, H.K. Exports (Ahmedabad, India) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for natural mukhawas (mouth freshner), published by FDA on January 11, 2022, 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
- Betel nut, shelled · UNSAFE ADD
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for H.K. Exports
6 records, newest first. Each line links to the FDA page it came from.
2024
- Import refusalRefused, Betel nut, shelledUNSAFE ADDUNSFDIETUSLACKS FIRMUSUAL NAMEPOISONORDEntry KM6-3624576-3Source
- Import refusalRefused, Betel nut, shelledPOISONORDEntry KM6-3626847-6Source
- Import refusalRefused, Mixed spice and seaonings, without salt, n.e.c.UNSAFE COLEntry KM6-3626847-6Source
2022
- Import refusalRefused, Mixed spice and seaonings, without salt, n.e.c.UNSAFE COLEntry KM6-3588770-6Source
- Import alert listingListed on Import Alert 45-02red listNatural mukhawas (mouth freshner)Source
2021
- Import refusalRefused, Mixed spice and seaonings, without salt, n.e.c.UNSAFE COLLIST INGRECOLOR LBLGEntry KM6-3564100-4Source
Refusal charges, in plain English
- UNSAFE COL3 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.
- POISONORD2 refused lines
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.
- COLOR LBLG1 refused line
Artificial coloring not declared
The product appeared to contain an artificial coloring without labeling that states that fact.
- 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).
- 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.
- UNSFDIETUS1 refused line
UNSFDIETUS
- USUAL NAME1 refused line
Common or usual name missing
The label appeared not to show the common or usual name of the food.
Questions about H.K. Exports
- Is H.K. Exports on an FDA import alert?
- Yes. As of October 26, 2026, H.K. Exports is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for natural mukhawas (mouth freshner); FDA published the listing on January 11, 2022.
- Has FDA refused shipments from H.K. Exports?
- Yes. FDA refused 5 shipment lines from H.K. Exports between December 14, 2021 and September 10, 2024. The most recent, on September 10, 2024, was betel nut, shelled, charged as UNSAFE ADD (food additive unsafe under section 409).
- Why did FDA refuse H.K. Exports's shipments?
- The most frequent charges are UNSAFE COL (color additive unsafe under section 721, 3 lines) and POISONORD (poisonous or deleterious substance (ordinarily injurious), 2 lines).
- What is H.K. Exports's FEI number?
- H.K. Exports's FDA Establishment Identifier (FEI) is 3010326532.
- Can shipments from H.K. Exports still enter the U.S.?
- Shipments of natural mukhawas (mouth freshner) from H.K. Exports 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.