Arcor DO Brasil LTDA
⚠️ Moderate Risk
FEI: 3003255928 • Braganca Paulista, Sao Paulo • BRAZIL
FEI Number
3003255928
Location
Braganca Paulista, Sao Paulo
Country
BRAZILAddress
Estrada Municipal Fulvio Salvador Pagani, 1301, Curitibanos, Braganca Paulista, Sao Paulo, 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
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)).
COLOR LBLG
The article appears to contain an artificial coloring and it fails to bear labeling stating that fact.
ALLERGEN
the label fails to declare all major food allergens present in the product, as required by section 403(w)(1).
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.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 8/21/2019 | 33YGT99CANDY WITHOUT CHOCOLATE N.E.C. | Division of Southeast Imports (DSEI) | |
| 8/21/2019 | 33EGT99HARD CANDY WITHOUT NUTS AND FRUIT, N.E.C. (WITHOUT CHOCOLATE) | Division of Southeast Imports (DSEI) | |
| 8/21/2019 | 34EGT02CHOCOLATE CANDY PIECES, WITH FRUIT AND FRUIT PRODUCTS | Division of Southeast Imports (DSEI) | |
| 8/21/2019 | 33CGT05CANDY BAR OR PIECES (NOT CARAMEL OR FONDANT), HARD, WITH FRUIT (WITHOUT CHOCOLATE) | Division of Southeast Imports (DSEI) | |
| 12/5/2017 | 34FGT02CHOCOLATE CANDY PIECES, WITHOUT NUTS AND FRUIT | Division of Northeast Imports (DNEI) | |
| 12/1/2017 | 33UFT02CHEWING GUM (WITHOUT CHOCOLATE) | 324NO ENGLISH | Division of Northeast Imports (DNEI) |
| 12/1/2017 | 33UFT02CHEWING GUM (WITHOUT CHOCOLATE) | 324NO ENGLISH | Division of Northeast Imports (DNEI) |
| 10/20/2017 | 34KYT04CHOCOLATE BARS | 324NO ENGLISH | Division of Northeast Imports (DNEI) |
| 10/20/2017 | 33UFT02CHEWING GUM (WITHOUT CHOCOLATE) | 324NO ENGLISH | Division of Northeast Imports (DNEI) |
Frequently Asked Questions
What is Arcor DO Brasil LTDA's FDA import refusal history?
Arcor DO Brasil LTDA (FEI: 3003255928) has 9 FDA import refusal record(s) in our database, spanning from 10/20/2017 to 8/21/2019.
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. Arcor DO Brasil LTDA's FEI number is 3003255928.
What types of violations has Arcor DO Brasil LTDA received?
Arcor DO Brasil LTDA has been cited for 4 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 Arcor DO Brasil LTDA come from?
All FDA import refusal data for Arcor DO Brasil 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.