EFX Importacao e Exportacao LTDA
⚠️ Moderate Risk
FEI: 3012966885 • Rio De Janeiro, Rio de Janeiro • BRAZIL
FEI Number
3012966885
Location
Rio De Janeiro, Rio de Janeiro
Country
BRAZILAddress
Avenida Brasil, 20204, Coelho Neto, Rio De Janeiro, Rio de Janeiro, Brazil
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
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.
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.
COLOR LBLG
The article appears to contain an artificial coloring and it fails to bear labeling stating that fact.
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).
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)).
FRNMFGREG
The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be misbranded as defined in section 502(o) of the FD&C Act. It appears that it was manufactured, prepared, propagated, compounded, or processed in an establishment not duly registered under section 510 of the Act.
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.
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.
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).
HEALTH C
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 bears an unauthorized nutrient content/health claim.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 8/4/2022 | 85NRCPADS, MENSTRUAL, SCENTED-DEODORIZED | 3280FRNMFGREG | Division of Northeast Imports (DNEI) |
| 1/7/2021 | 28BGT54PEPPER, BLACK, GROUND, CRACKED (SPICE) | 9SALMONELLA | Division of Northeast Imports (DNEI) |
| 1/7/2021 | 28BGT54PEPPER, BLACK, GROUND, CRACKED (SPICE) | 9SALMONELLA | Division of Northeast Imports (DNEI) |
| 1/7/2021 | 28BGT54PEPPER, BLACK, GROUND, CRACKED (SPICE) | 9SALMONELLA | Division of Northeast Imports (DNEI) |
| 7/20/2016 | 62FBL17HYDROGEN PEROXIDE (SOL) (ANTI-INFECTIVE, TOPICAL) | Division of Northeast Imports (DNEI) | |
| 6/27/2016 | 21ACE26OTHER FRUITS AND SUBTROPICAL/TROPICAL FRUIT, MIXED | Division of Northeast Imports (DNEI) | |
| 6/27/2016 | 21ACE21PIT AND SUBTROPICAL/TROPICAL, MIXED | Division of Northeast Imports (DNEI) | |
| 2/10/2016 | 30JFT99IMITATION FRUIT FLAVORED BEVERAGE BASE, N.E.C. | Division of Northeast Imports (DNEI) | |
| 2/10/2016 | 30JFT99IMITATION FRUIT FLAVORED BEVERAGE BASE, N.E.C. | Division of Northeast Imports (DNEI) | |
| 2/10/2016 | 03YGT99OTHER BAKERY PRODUCTS, N.E.C. | Division of Northeast Imports (DNEI) | |
| 2/10/2016 | 03YGT99OTHER BAKERY PRODUCTS, N.E.C. | Division of Northeast Imports (DNEI) | |
| 2/10/2016 | 30JFT99IMITATION FRUIT FLAVORED BEVERAGE BASE, N.E.C. | Division of Northeast Imports (DNEI) | |
| 2/10/2016 | 30JFT99IMITATION FRUIT FLAVORED BEVERAGE BASE, N.E.C. | Division of Northeast Imports (DNEI) |
Frequently Asked Questions
What is EFX Importacao e Exportacao LTDA's FDA import refusal history?
EFX Importacao e Exportacao LTDA (FEI: 3012966885) has 13 FDA import refusal record(s) in our database, spanning from 2/10/2016 to 8/4/2022.
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. EFX Importacao e Exportacao LTDA's FEI number is 3012966885.
What types of violations has EFX Importacao e Exportacao LTDA received?
EFX Importacao e Exportacao LTDA has been cited for 12 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 EFX Importacao e Exportacao LTDA come from?
All FDA import refusal data for EFX Importacao e Exportacao LTDA 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.