Liquid Lens
⚠️ Moderate Risk
FEI: 3009203585 • Leighton Buzzardleighton Buzzard • UNITED KINGDOM
FEI Number
3009203585
Location
Leighton Buzzardleighton Buzzard
Country
UNITED KINGDOMAddress
Unit 4 Grovebury Placeleighton Buzzard, , Leighton Buzzardleighton Buzzard, , 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
COLOR LBLG
The article appears to contain an artificial coloring and it fails to bear labeling stating that fact.
UNSAFE ADD
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain an unsafe food additive within the meaning of section 409.
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.
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.
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.
FALSE
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(a)(1 ) of the FD&C Act in that the labeling is false or misleading in any particular.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 1/21/2014 | 33CHY07JELLIED CANDIES, HARD (JELLY BEANS, GUM DROPS, ETC.), WITH FRUIT (WITHOUT CHOCOLATE) | New York District Office (NYK-DO) | |
| 1/13/2014 | 33CHY07JELLIED CANDIES, HARD (JELLY BEANS, GUM DROPS, ETC.), WITH FRUIT (WITHOUT CHOCOLATE) | New Orleans District Office (NOL-DO) | |
| 11/25/2011 | 33LGE07JELLIED CANDY, SOFT (JELLY BEANS, GUM DROPS, ETC.), WITHOUT NUTS AND FRUIT (WITHOUT CHOCOLATE) | 274COLOR LBLG | New Orleans District Office (NOL-DO) |
Frequently Asked Questions
What is Liquid Lens's FDA import refusal history?
Liquid Lens (FEI: 3009203585) has 3 FDA import refusal record(s) in our database, spanning from 11/25/2011 to 1/21/2014.
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. Liquid Lens's FEI number is 3009203585.
What types of violations has Liquid Lens received?
Liquid Lens has been cited for 7 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 Liquid Lens come from?
All FDA import refusal data for Liquid Lens 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.