Lucozade Ribena Suntory Ltd
⚠️ Moderate Risk
FEI: 3011721955 • Uxbridge, Middlesex • UNITED KINGDOM
FEI Number
3011721955
Location
Uxbridge, Middlesex
Country
UNITED KINGDOMAddress
2 Longwalk Road, , Uxbridge, Middlesex, 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
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).
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.
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.
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.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 2/4/2022 | 20DGT29CURRANTS, BLACK CASSIS, JUICES OR CONCENTRATES | 11UNSAFE COL | Division of West Coast Imports (DWCI) |
| 2/4/2022 | 29BGT01SOFT DRINK, BERRY FRUIT FLAVORED, CARBONATED | 11UNSAFE COL | Division of Southwest Imports (DSWI) |
| 5/12/2020 | 29BGT01SOFT DRINK, BERRY FRUIT FLAVORED, CARBONATED | 11UNSAFE COL | Division of Northeast Imports (DNEI) |
| 5/12/2020 | 29BGT01SOFT DRINK, BERRY FRUIT FLAVORED, CARBONATED | 11UNSAFE COL | Division of Northeast Imports (DNEI) |
| 5/25/2017 | 20DCT29CURRANTS, BLACK CASSIS, JUICES OR CONCENTRATES | 11UNSAFE COL | Division of Northeast Imports (DNEI) |
| 11/23/2016 | 29BGT99CARBONATED SOFT DRINK, N.E.C. | 320LACKS FIRM | Division of Northeast Imports (DNEI) |
| 11/23/2016 | 29BGT99CARBONATED SOFT DRINK, N.E.C. | 320LACKS FIRM | Division of Northeast Imports (DNEI) |
| 10/5/2016 | 20DHO29CURRANTS, BLACK CASSIS, JUICES OR CONCENTRATES | Division of Southwest Imports (DSWI) | |
| 8/20/2015 | 29BGT99CARBONATED SOFT DRINK, N.E.C. | Division of Northeast Imports (DNEI) |
Frequently Asked Questions
What is Lucozade Ribena Suntory Ltd's FDA import refusal history?
Lucozade Ribena Suntory Ltd (FEI: 3011721955) has 9 FDA import refusal record(s) in our database, spanning from 8/20/2015 to 2/4/2022.
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. Lucozade Ribena Suntory Ltd's FEI number is 3011721955.
What types of violations has Lucozade Ribena Suntory Ltd received?
Lucozade Ribena Suntory Ltd has been cited for 5 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 Lucozade Ribena Suntory Ltd come from?
All FDA import refusal data for Lucozade Ribena Suntory Ltd 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.