Fayus Enterprises
⚠️ High Risk
FEI: 1000445973 • Lagos, Lagos • NIGERIA
FEI Number
1000445973
Location
Lagos, Lagos
Country
NIGERIAAddress
46 Babatunde Ladega St., , Lagos, Lagos, Nigeria
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
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.
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.
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.
SALMONELLA
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain Salmonella, a poisonous and deleterious substance which may render it injurious to health.
EPHEDALK
The product is subject to refusal of admission pursuant to Section 801(a)(3) in that it is a dietary supplement or a dietary ingredient that appears to contain ephedrine alkaloids, which presents an unreasonable risk of illness or injury under the conditions of use recommended or suggested in the labeling, or if no conditions of use are suggested in the labeling, under ordinary conditions of use.
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.
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).
LABELING
The article appears in violation of FPLA because of its placement, form and/or contents statement.
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).
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.
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).
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.
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.
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.
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).
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.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 12/23/2024 | 25YGT99VEGETABLE & VEGETABLE PRODUCTS NOT MENTIONED ELSEWHERE, N.E.C. | 249FILTHY | Division of Northeast Imports (DNEI) |
| 9/9/2024 | 02HGT99STARCH PRODUCTS N.E.C. | Division of Northeast Imports (DNEI) | |
| 9/9/2024 | 02GGT99FLOURS AND MEALS N.E.C. | Division of Northeast Imports (DNEI) | |
| 6/11/2024 | 02HYT01TAPIOCA STARCH PRODUCT | 9SALMONELLA | Division of Northeast Imports (DNEI) |
| 4/4/2024 | 28KAH99SPICES AND SEASONING, GROUND, CRACKED, WITH SALT, N.E.C. | Division of West Coast Imports (DWCI) | |
| 7/25/2023 | 54FYY09EPHEDRA (HERBAL & BOTANICALS, NOT TEAS) | 3120EPHEDALK | Division of West Coast Imports (DWCI) |
| 7/25/2023 | 54FYY09EPHEDRA (HERBAL & BOTANICALS, NOT TEAS) | 3120EPHEDALK | Division of West Coast Imports (DWCI) |
| 8/5/2016 | 05BFT99BREAKFAST FOOD QUICK OR INSTANT COOKING, N.E.C. | Division of West Coast Imports (DWCI) | |
| 8/5/2016 | 05BFT99BREAKFAST FOOD QUICK OR INSTANT COOKING, N.E.C. | Division of West Coast Imports (DWCI) | |
| 5/24/2016 | 02HFT02CORN STARCH | Division of West Coast Imports (DWCI) | |
| 6/10/2005 | 21VCE24PALM NUT (PALM FRUIT, SUGAR PALM), JUICE, MILK, CREME, DRINK OR NECTAR, SUB/TROPICAL FRUIT | San Francisco District Office (SAN-DO) | |
| 2/23/2005 | 21VCE24PALM NUT (PALM FRUIT, SUGAR PALM), JUICE, MILK, CREME, DRINK OR NECTAR, SUB/TROPICAL FRUIT | San Francisco District Office (SAN-DO) | |
| 5/17/2004 | 66VBL99MISCELLANEOUS PATENT MEDICINES, ETC. | San Francisco District Office (SAN-DO) | |
| 5/17/2004 | 66VBL99MISCELLANEOUS PATENT MEDICINES, ETC. | San Francisco District Office (SAN-DO) |
Frequently Asked Questions
What is Fayus Enterprises's FDA import refusal history?
Fayus Enterprises (FEI: 1000445973) has 14 FDA import refusal record(s) in our database, spanning from 5/17/2004 to 12/23/2024.
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. Fayus Enterprises's FEI number is 1000445973.
What types of violations has Fayus Enterprises received?
Fayus Enterprises has been cited for 16 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 Fayus Enterprises come from?
All FDA import refusal data for Fayus Enterprises 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.