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Dongguan HengWenXin Inc.

FDA import alert and refusal historyDongguan, ChinaFEI 3018741039

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Example subjectDongguan HengWenXin Inc added to Import Alert 16-129 (red list)

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As of October 26, 2026, Dongguan HengWenXin Inc. (Dongguan, China) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for "weilong kiss burn" instant gluten; spicy fried gluten snack, published by FDA on February 1, 2022, and has 8 FDA import refusals recorded since October 2016.

Data from FDA public records, last checked . Request a correction

Current status

Last import refusal
Soft drinks and waters not mentioned elsewhere, n.e.c. · MELAMINE
Last warning letter
None found
Last inspection
None on record

Every FDA record for Dongguan HengWenXin Inc.

9 records, newest first. Each line links to the FDA page it came from.

2022

  1. Import alert listing
    Listed on Import Alert 45-02red list"Weilong Kiss Burn" Instant Gluten; Spicy Fried Gluten Snack
    Source
  2. Import refusal
    Refused, 8 lines in one entry: Soft drinks and waters not mentioned elsewhere, n.e.c.; Baked snack food, n.e.c. and 1 moreMELAMINENO ENGLISHALLERGENNUTRIT LBLEntry NDX-0302080-7Show 8 lines
    Source

Refusal charges, in plain English

  • MELAMINE7 refused lines

    Melamine

    The product appeared to contain melamine or a melamine analog, which is an unsafe food additive within the meaning of section 409 of the FD&C Act.

  • ALLERGEN5 refused lines

    Major food allergen not declared

    The label appeared not to declare all major food allergens present in the product, as section 403(w) of the FD&C Act requires.

  • NUTRIT LBL5 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.

  • NO ENGLISH4 refused lines

    Required label information not in English

    Information that must appear on the label appeared not to be given in English, or not to be repeated in every language used on the label.

  • NO PROCESS3 refused lines

    No scheduled process filed

    The manufacturer appeared not to have filed a scheduled process with FDA, which 21 CFR Part 108 requires for low-acid canned and acidified foods, so the product is treated as made under insanitary conditions.

  • FLAVR LBLG2 refused lines

    FLAVR LBLG

  • LIST INGRE2 refused lines

    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 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.

Questions about Dongguan HengWenXin Inc.

Is Dongguan HengWenXin Inc. on an FDA import alert?
Yes. As of October 26, 2026, Dongguan HengWenXin Inc. is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for "weilong kiss burn" instant gluten; spicy fried gluten snack; FDA published the listing on February 1, 2022.
Has FDA refused shipments from Dongguan HengWenXin Inc.?
Yes. FDA refused 8 shipment lines from Dongguan HengWenXin Inc. on January 25, 2022. The most recent, on January 25, 2022, was soft drinks and waters not mentioned elsewhere, n.e.c., charged as MELAMINE (melamine).
Why did FDA refuse Dongguan HengWenXin Inc.'s shipments?
The most frequent charges are MELAMINE (melamine, 7 lines) and ALLERGEN (major food allergen not declared, 5 lines).
What is Dongguan HengWenXin Inc.'s FEI number?
Dongguan HengWenXin Inc.'s FDA Establishment Identifier (FEI) is 3018741039.
Can shipments from Dongguan HengWenXin Inc. still enter the U.S.?
Shipments of "weilong kiss burn" instant gluten; spicy fried gluten snack from Dongguan HengWenXin Inc. 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.