Jiang Men Cutlery Manufactory
⚠️ High Risk
FEI: 1000291348 • Jiang Men • 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
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.
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).
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.
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).
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.
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).
INSANITARY
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to have been prepared, packed, or held under insanitary conditions whereby it may have become contaminated with filth, or whereby it may have been rendered injurious to health.
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.
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)).
TRANSFAT
The product is misbranded under Section 403(q) because the nutrition label does not provide all of the information required by 21 CFR 101.9(c); specifically, the label does not bear the amount of trans fat [21 CFR 101.9(c)(2)(ii)].
LACKS N/C
The article is in package form and appears to not have a label containing an accurate statement of the quantity of the contents in terms of weight, measure or numerical count and no variations or exemptions have been prescribed by regs.
FOREIGN OB
The article appears to consist in whole or in part of a filthy, putrid, or decomposed substance, or is otherwise unfit for food in that it appears to contain foreign objects.
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.
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).
COLOR LBLG
The article appears to contain an artificial coloring and it fails to bear labeling stating that fact.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 12/9/2009 | 54FCT99HERBALS & BOTANICALS (NOT TEAS), N.E.C. | 249FILTHY | Los Angeles District Office (LOS-DO) |
| 10/14/2008 | 24HGH99FRUITS USED AS VEGETABLES, DRIED OR PASTE, N.E.C. | 249FILTHY | Los Angeles District Office (LOS-DO) |
| 10/14/2008 | 24HGH99FRUITS USED AS VEGETABLES, DRIED OR PASTE, N.E.C. | 249FILTHY | Los Angeles District Office (LOS-DO) |
| 9/23/2008 | 37BCT32BEAN CURD, N.E.C. (MULTIPLE FOOD SPECIALTIES, SIDE DISHES & DESSERTS) | 249FILTHY | Los Angeles District Office (LOS-DO) |
| 8/1/2008 | 03FGT08SHRIMP/PRAWN CRACKERS | Los Angeles District Office (LOS-DO) | |
| 8/23/2007 | 28AGH08CAPSICUMS (CAYENNE CHILI, HOT PEPPERS), WHOLE (SPICE) | 249FILTHY | Los Angeles District Office (LOS-DO) |
| 8/23/2007 | 28AGH08CAPSICUMS (CAYENNE CHILI, HOT PEPPERS), WHOLE (SPICE) | 249FILTHY | Los Angeles District Office (LOS-DO) |
| 8/23/2007 | 28AGH08CAPSICUMS (CAYENNE CHILI, HOT PEPPERS), WHOLE (SPICE) | 249FILTHY | Los Angeles District Office (LOS-DO) |
| 8/23/2007 | 28AGH08CAPSICUMS (CAYENNE CHILI, HOT PEPPERS), WHOLE (SPICE) | 249FILTHY | Los Angeles District Office (LOS-DO) |
| 5/9/2007 | 24TGT08CABBAGE (LEAF & STEM VEGETABLE) | Los Angeles District Office (LOS-DO) | |
| 2/12/2007 | 24HGH99FRUITS USED AS VEGETABLES, DRIED OR PASTE, N.E.C. | Los Angeles District Office (LOS-DO) | |
| 2/12/2007 | 24HGH99FRUITS USED AS VEGETABLES, DRIED OR PASTE, N.E.C. | 249FILTHY | Los Angeles District Office (LOS-DO) |
| 2/12/2007 | 28AGH18FENNEL, WHOLE (SPICE) | 157FOREIGN OB | Los Angeles District Office (LOS-DO) |
| 3/14/2006 | 30GCT99BEVERAGE BASE OF NON-FRUIT ORIGIN, LIQUID, N.E.C. | Los Angeles District Office (LOS-DO) | |
| 12/7/2005 | 04CGT04NOODLES, VEGETABLE | 249FILTHY | Los Angeles District Office (LOS-DO) |
| 12/7/2005 | 54FCT06CHRYSANTHEMUM (HERBAL & BOTANICALS, NOT TEAS) | Los Angeles District Office (LOS-DO) | |
| 12/7/2005 | 03FGT08SHRIMP/PRAWN CRACKERS | Los Angeles District Office (LOS-DO) | |
| 9/13/2005 | 37BCE32BEAN CURD, N.E.C. (MULTIPLE FOOD SPECIALTIES, SIDE DISHES & DESSERTS) | Los Angeles District Office (LOS-DO) | |
| 7/6/2005 | 21HGT05DATES, DRIED OR PASTE | 249FILTHY | Los Angeles District Office (LOS-DO) |
| 6/7/2005 | 24UGH99LEAF & STEM VEGETABLES, DRIED OR PASTE, N.E.C. | Los Angeles District Office (LOS-DO) | |
| 6/25/2004 | 37BCP27BEAN CURD, FRESH - SOFT OR HARD (MULTIPLE FOOD SPECIALTIES, SIDE DISHES AND DESSERTS) | Los Angeles District Office (LOS-DO) | |
| 6/25/2004 | 37BGP30BEAN CURD CUBES, FERMENTED (E.G., SALTED) IN OIL/SAUCE/ WINE, ETC. (MULT FOOD SPEC/SIDE DISH/DESSERT | Los Angeles District Office (LOS-DO) | |
| 6/25/2004 | 37BGP30BEAN CURD CUBES, FERMENTED (E.G., SALTED) IN OIL/SAUCE/ WINE, ETC. (MULT FOOD SPEC/SIDE DISH/DESSERT | Los Angeles District Office (LOS-DO) |
Frequently Asked Questions
What is Jiang Men Cutlery Manufactory's FDA import refusal history?
Jiang Men Cutlery Manufactory (FEI: 1000291348) has 23 FDA import refusal record(s) in our database, spanning from 6/25/2004 to 12/9/2009.
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. Jiang Men Cutlery Manufactory's FEI number is 1000291348.
What types of violations has Jiang Men Cutlery Manufactory received?
Jiang Men Cutlery Manufactory has been cited for 15 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 Jiang Men Cutlery Manufactory come from?
All FDA import refusal data for Jiang Men Cutlery Manufactory 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.