UNILEVER UK LIMITED
⚠️ Moderate Risk
FEI: 3013420180 • Leatherhead, Surrey • UNITED KINGDOM
FEI Number
3013420180
Location
Leatherhead, Surrey
Country
UNITED KINGDOMAddress
Unilever House, Springfield Drive, Leatherhead, Surrey, United Kingdom
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
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).
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.
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.
NO ENGLISH
Required label or labeling appears to not be in English in violation of 21 C.F.R. 201.15(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.
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.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 8/6/2024 | 62WBY99ASTRINGENT/ANTI-PERSPIRANT N.E.C. | Division of Southeast Imports (DSEI) | |
| 8/6/2024 | 62WBY99ASTRINGENT/ANTI-PERSPIRANT N.E.C. | Division of Southeast Imports (DSEI) | |
| 9/23/2020 | 62HAL05ETHYL ALCOHOL (ANTI-MICROBIAL) | Division of Southeast Imports (DSEI) | |
| 1/13/2016 | 31KGT01TEA, BLACK | 328USUAL NAME | New Orleans District Office (NOL-DO) |
| 2/24/2015 | 27YCT05MUSTARD, PREPARED | Division of Southeast Imports (DSEI) | |
| 2/24/2015 | 31KFT01TEA, BLACK | Division of Southeast Imports (DSEI) |
Frequently Asked Questions
What is UNILEVER UK LIMITED's FDA import refusal history?
UNILEVER UK LIMITED (FEI: 3013420180) has 6 FDA import refusal record(s) in our database, spanning from 2/24/2015 to 8/6/2024.
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. UNILEVER UK LIMITED's FEI number is 3013420180.
What types of violations has UNILEVER UK LIMITED received?
UNILEVER UK LIMITED has been cited for 6 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 UNILEVER UK LIMITED come from?
All FDA import refusal data for UNILEVER UK LIMITED 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.