Macat Group Foodstuff Corporation Ltd.
⚠️ Moderate Risk
FEI: 3004257401 • Huizhou, Guangdong • CHINA
FEI Number
3004257401
Location
Huizhou, Guangdong
Country
CHINAAddress
Macat Bldgs F/8, No. 63 Maidi Road, Huizhou, Guangdong, China
Moderate Risk
FDA Import Risk Assessment
This firm has a moderate history of FDA import refusals. Some attention may be warranted.
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
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.
NOT LISTED
It appears the drug or device is not included in a list required by Section 510(j), or a notice or other information respecting it was not provided as required by section 510(j) or 510(k).
UNAPPROVED
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a new drug within the meaning of Section 201(p) without an approved New Drug Application (NDA).
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).
CYCLAMATE
The article appears to bear or contain cyclamate, an unsafe food additive within the meaning of Section 409
DULCIN
The article appears to bear or contain dulcin, an unsafe food additive within the meaning of Section 409
NO ENGLISH
Required label or labeling appears to not be in English in violation of 21 C.F.R. 201.15(c)(1).
SACCHARLBL
The article contains Saccharin, a non-nutritive sweetener, and its label or labeling fails to list it as an added ingredient
DIRECTIONS
The article is subject to refusal of admission pursuant to section 801(a)(3) in that it is a device whose label appears to not bear adequate directions for use.
COLOR LBLG
The article appears to contain an artificial coloring and it fails to bear labeling stating that fact.
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.
LACKS N/C
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)(2) of the FD&C Act in that the food is in package form and the label fails to bear an accurate statement of the quantity of the contents in terms of weight, measure, or numerical count in accordance with Section 403(e)(2) of the FD&C Act.
NO ENGLISH
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(f) of the FD&C Act in that any word, statement, or other information required by or under the authority of the FD&C Act to appear on the label or labeling is not prominently placed thereon with such conspicuousness (as compared with other words, statements, designs, or devices, in the labeling) and in such terms as to render it likely to be read and understood by the ordinary individual under customary terms of purchase and use (for example, label contains information in two or more languages but fails to repeat all required information in both languages in accordance with 21 CFR 101.15(c)(2), or label fails to include all required information in English in accordance with 21 CFR 101.15(c)(1), except in the case of articles distributed solely in the Commonwealth of Puerto Rico or in a Territory where the predominant language is one other than English)).
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.
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.
FALSE
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(a)(1 ) of the FD&C Act in that the labeling is false or misleading in any particular.
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).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 7/21/2010 | 20HGH09TANGERINE, DRIED OR PASTE | New York District Office (NYK-DO) | |
| 3/26/2009 | 21HGT01APRICOT, DRIED OR PASTE | 2720DULCIN | New York District Office (NYK-DO) |
| 3/26/2009 | 21HGT01APRICOT, DRIED OR PASTE | 2640CYCLAMATE | New York District Office (NYK-DO) |
| 12/1/2008 | 25JGP14TURNIP (ROOT & TUBER VEGETABLE) | 324NO ENGLISH | San Francisco District Office (SAN-DO) |
| 10/27/2007 | 63HAR99CATHARTIC N.E.C. | San Francisco District Office (SAN-DO) | |
| 10/10/2007 | 21HGT05DATES, DRIED OR PASTE | 249FILTHY | San Francisco District Office (SAN-DO) |
| 10/10/2007 | 21HGT05DATES, DRIED OR PASTE | 249FILTHY | San Francisco District Office (SAN-DO) |
| 4/28/2007 | 62UAY99ANTI-TUSSIVE/COLD N.E.C. | San Francisco District Office (SAN-DO) | |
| 4/10/2007 | 25SGH01MUSHROOM, COMMON (AGARICUS BISPORUS), FUNGI PRODUCTS, N.E.C. | 249FILTHY | San Francisco District Office (SAN-DO) |
| 4/10/2007 | 66VBY99MISCELLANEOUS PATENT MEDICINES, ETC. | 118NOT LISTED | San Francisco District Office (SAN-DO) |
| 3/13/2007 | 54EGT99HERBALS & BOTANICAL TEAS, N.E.C. | San Francisco District Office (SAN-DO) | |
| 1/22/2007 | 37CFH28BEAN CURD, DRIED (STICKS, SHEETS), (PACKAGE CONTAINS SEPARATE COMPONENTS REQUIRING MIX/COOK PREP | San Francisco District Office (SAN-DO) | |
| 1/22/2007 | 21HFT14PLUM, DRIED OR PASTE | San Francisco District Office (SAN-DO) | |
| 6/3/2004 | 25JGT14TURNIP (ROOT & TUBER VEGETABLE) | San Francisco District Office (SAN-DO) |
Frequently Asked Questions
What is Macat Group Foodstuff Corporation Ltd.'s FDA import refusal history?
Macat Group Foodstuff Corporation Ltd. (FEI: 3004257401) has 14 FDA import refusal record(s) in our database, spanning from 6/3/2004 to 7/21/2010.
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. Macat Group Foodstuff Corporation Ltd.'s FEI number is 3004257401.
What types of violations has Macat Group Foodstuff Corporation Ltd. received?
Macat Group Foodstuff Corporation 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 Macat Group Foodstuff Corporation Ltd. come from?
All FDA import refusal data for Macat Group Foodstuff Corporation 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.