JIANGMEN CHANGHAO IMP.&EXP.CO.,LTD
⚠️ High Risk
FEI: 3013388491 • Jiangmen, Guangdong • CHINA
FEI Number
3013388491
Location
Jiangmen, Guangdong
Country
CHINAAddress
Xinhui District Room 108, Block 1,No 105,Sanhe Road North, Jiangmen, Guangdong, China
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
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.
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.
UNSAFE COL
The article appears to be, or to bear or contain a color additive which is unsafe within the meaning of Section 721(a).
MELAMINE
The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to bear or contain a food additive, namely melamine and/or a melamine analog, that is unsafe within the meaning of section 409.
ALLERGEN
the label fails to declare all major food allergens present in the product, as required by section 403(w)(1).
NO PROCESS
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the manufacturer's failure to file a scheduled process demonstrates that the product is not being manufactured under the mandatory provisions of 21 CFR Part 108 and therefore appears to have been manufactured, processed, or packed, under insanitary conditions whereby it may have been rendered injurious to health.
POISONOUS
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain a poisonous or deleterious substance which may render the article injurious to health. Contains:
CYCLAMATE
The article appears to bear or contain cyclamate, an unsafe food additive within the meaning of Section 409
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.
LACKS FIRM
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)(1) of the FD&C Act in that the food is in package form and the label fails to bear the name and place of business of the manufacturer, packer, or distributor.
AFLATOXIN
The article appears to contain a mycotoxin, a poisonous and deleterious substance which may render it injurious to health.
ALRGN402A4
it appears to be adulterated within the meaning of section 402(a)(4) because it appears that the food was prepared, packed, or held under insanitary conditions whereby it may have been rendered injurious to health, specifically because the food appears to contain a major food allergen through insanitary conditions that led to cross-contact.
SACCHARLBL
The article appears to contain Saccharin, a non-nutritive sweetener, and its label or labeling fails to list it as an added ingredient.
NUTRIT LBL
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 fails to bear the required nutrition information.
NEEDS FCE
It appears the manufacturer is not registered as a low acid canned food or acidified food manufacturer pursuant to 21 CFR 108.25(c)(1) or 108.35(c)(1).
YELLOW #5
The food appears to bear or contain the color additive FD & C Yellow No. 5, which is not declared on the label per 21 CFR 74.705(a)(c) under section 721.
DULCIN
The article appears to bear or contain dulcin, an unsafe food additive within the meaning of Section 409
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 10/11/2024 | 28YYT99SPICES, FLAVORS AND SALT NOT MENTIONED ELSEWHERE, N.E.C. | 251POISONOUS | Division of Northeast Imports (DNEI) |
| 9/13/2024 | 31KFH02TEA, GREEN | Division of Northeast Imports (DNEI) | |
| 2/12/2024 | 21HGH05DATES, DRIED OR PASTE | 249FILTHY | Division of Northeast Imports (DNEI) |
| 11/8/2021 | 03YYY99OTHER BAKERY PRODUCTS, N.E.C. | Division of Northeast Imports (DNEI) | |
| 11/8/2021 | 03HGY07MIXED PLAIN COOKIES,BISCUITS AND WAFERS | Division of Northeast Imports (DNEI) | |
| 11/8/2021 | 07BGT99FRIED SNACK FOODS, N.E.C. | Division of Northeast Imports (DNEI) | |
| 11/8/2021 | 07BGT99FRIED SNACK FOODS, N.E.C. | Division of Northeast Imports (DNEI) | |
| 3/29/2021 | 03HGT08BUTTER/BUTTER FLAVORED,PLAIN COOKIES,BISCUITS AND WAFERS | 3421MELAMINE | Division of West Coast Imports (DWCI) |
| 10/22/2020 | 21HYY05DATES, DRIED OR PASTE | 249FILTHY | Division of Northeast Imports (DNEI) |
| 9/23/2020 | 37JYY99SAUCES, N.E.C. | Division of Northeast Imports (DNEI) | |
| 8/16/2018 | 21HGT16CHINESE RED DATE (JUJUBES, ZIZIPHUS JUJUBA), DRIED OR PASTE | Division of Northeast Imports (DNEI) | |
| 10/6/2015 | 03RYY02CAKES, FILLED (OTHER THAN FRUIT OR JELLY) | Division of Northeast Imports (DNEI) | |
| 7/20/2012 | 33CGT13ROCK CANDY, HARD, WITH FRUIT (WITHOUT CHOCOLATE) | 2640CYCLAMATE | Division of Northeast Imports (DNEI) |
| 5/31/2012 | 04CGT09NOODLES, IMITATION | 482NUTRIT LBL | Division of Northeast Imports (DNEI) |
| 4/14/2011 | 21HGH05DATES, DRIED OR PASTE | 11UNSAFE COL | New York District Office (NYK-DO) |
| 4/14/2011 | 21HGH05DATES, DRIED OR PASTE | 11UNSAFE COL | New York District Office (NYK-DO) |
| 1/13/2011 | 03FGT02FLAVORED OR PARTY CRACKERS | New York District Office (NYK-DO) | |
| 12/7/2010 | 33EFT12MIXED/ASSORTED HARD CANDY WITHOUT NUTS AND FRUIT (WITHOUT CHOCOLATE) | New York District Office (NYK-DO) | |
| 7/20/2010 | 25PGT09FUNGUS, BLACK (CLOUD EARS), WHOLE (BUTTON) (FUNGI) | 249FILTHY | New York District Office (NYK-DO) |
| 8/23/2005 | 33SFH99CANDY SPECIALTIES, N.E.C. (WITHOUT CHOCOLATE) | 320LACKS FIRM | New York District Office (NYK-DO) |
| 7/29/2005 | 23BGT99NUT, SHELLED, N.E.C. | 297AFLATOXIN | New York District Office (NYK-DO) |
| 7/29/2005 | 54FYT99HERBALS & BOTANICALS (NOT TEAS), N.E.C. | 249FILTHY | New York District Office (NYK-DO) |
| 7/29/2005 | 28AGT99WHOLE SPICE, N.E.C. | 249FILTHY | New York District Office (NYK-DO) |
Frequently Asked Questions
What is JIANGMEN CHANGHAO IMP.&EXP.CO.,LTD's FDA import refusal history?
JIANGMEN CHANGHAO IMP.&EXP.CO.,LTD (FEI: 3013388491) has 23 FDA import refusal record(s) in our database, spanning from 7/29/2005 to 10/11/2024.
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. JIANGMEN CHANGHAO IMP.&EXP.CO.,LTD's FEI number is 3013388491.
What types of violations has JIANGMEN CHANGHAO IMP.&EXP.CO.,LTD received?
JIANGMEN CHANGHAO IMP.&EXP.CO.,LTD has been cited for 17 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 JIANGMEN CHANGHAO IMP.&EXP.CO.,LTD come from?
All FDA import refusal data for JIANGMEN CHANGHAO IMP.&EXP.CO.,LTD 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.