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Fayus Enterprises

⚠️ High Risk

FEI: 1000445973 • Lagos, Lagos • NIGERIA

FEI

FEI Number

1000445973

📍

Location

Lagos, Lagos

🇳🇬

Country

NIGERIA
🏢

Address

46 Babatunde Ladega St., , Lagos, Lagos, Nigeria

High Risk

FDA Import Risk Assessment

55.2
LowModerateHighCritical

This firm has a significant history of FDA import refusals with notable violations.

Statistics

14
Total Refusals
16
Unique Violations
12/23/2024
Latest Refusal
5/17/2004
Earliest Refusal

Score Breakdown

Violation Severity
64.2×40%
Refusal Volume
43.6×30%
Recency
79.0×20%
Frequency
6.8×10%
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

3216×

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.

2494×

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.

832×

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.

92×

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.

31202×

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.

162×

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.

1182×

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).

4732×

LABELING

The article appears in violation of FPLA because of its placement, form and/or contents statement.

622×

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).

4822×

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.

752×

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).

3281×

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.

2181×

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.

3201×

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.

111×

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).

641×

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

DateProductViolationsDivision
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.
249FILTHY
321LACKS N/C
Division of Northeast Imports (DNEI)
9/9/2024
02GGT99FLOURS AND MEALS N.E.C.
249FILTHY
321LACKS N/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.
218LIST INGRE
249FILTHY
320LACKS FIRM
321LACKS N/C
328USUAL NAME
9SALMONELLA
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.
321LACKS N/C
482NUTRIT LBL
Division of West Coast Imports (DWCI)
8/5/2016
05BFT99BREAKFAST FOOD QUICK OR INSTANT COOKING, N.E.C.
321LACKS N/C
482NUTRIT LBL
Division of West Coast Imports (DWCI)
5/24/2016
02HFT02CORN STARCH
11UNSAFE COL
321LACKS N/C
64YELLOW #5
Division of West Coast Imports (DWCI)
6/10/2005
21VCE24PALM NUT (PALM FRUIT, SUGAR PALM), JUICE, MILK, CREME, DRINK OR NECTAR, SUB/TROPICAL FRUIT
62NEEDS FCE
83NO PROCESS
San Francisco District Office (SAN-DO)
2/23/2005
21VCE24PALM NUT (PALM FRUIT, SUGAR PALM), JUICE, MILK, CREME, DRINK OR NECTAR, SUB/TROPICAL FRUIT
62NEEDS FCE
83NO PROCESS
San Francisco District Office (SAN-DO)
5/17/2004
66VBL99MISCELLANEOUS PATENT MEDICINES, ETC.
118NOT LISTED
16DIRECTIONS
473LABELING
75UNAPPROVED
San Francisco District Office (SAN-DO)
5/17/2004
66VBL99MISCELLANEOUS PATENT MEDICINES, ETC.
118NOT LISTED
16DIRECTIONS
473LABELING
75UNAPPROVED
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.