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Cottage Delight Limited

⚠️ Moderate Risk

FEI: 3008446202 • Leek, Staffordshire • UNITED KINGDOM

FEI

FEI Number

3008446202

📍

Location

Leek, Staffordshire

🇬🇧
🏢

Address

Brooklands Way, Leekbrook Way, Leek, Staffordshire, United Kingdom

Moderate Risk

FDA Import Risk Assessment

36.4
LowModerateHighCritical

This firm has a moderate history of FDA import refusals. Some attention may be warranted.

Statistics

6
Total Refusals
4
Unique Violations
1/31/2015
Latest Refusal
1/17/2003
Earliest Refusal

Score Breakdown

Violation Severity
66.4×40%
Refusal Volume
31.3×30%
Recency
0.0×20%
Frequency
5.0×10%
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

2185×

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.

33004×

ALLERGEN

the label fails to declare all major food allergens present in the product, as required by section 403(w)(1).

111×

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).

831×

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.

Refusal History

DateProductViolationsDivision
1/31/2015
21CGT09OTHER FRUITS, MIXED, FLAVORED JAMS, JELLIES, PRESERVES, MARMALADES, BUTTERS AND CANDIED
218LIST INGRE
3300ALLERGEN
New England District Office (NWE-DO)
1/31/2015
21CGT09OTHER FRUITS, MIXED, FLAVORED JAMS, JELLIES, PRESERVES, MARMALADES, BUTTERS AND CANDIED
218LIST INGRE
3300ALLERGEN
New England District Office (NWE-DO)
1/31/2015
21CGT09OTHER FRUITS, MIXED, FLAVORED JAMS, JELLIES, PRESERVES, MARMALADES, BUTTERS AND CANDIED
218LIST INGRE
3300ALLERGEN
New England District Office (NWE-DO)
1/31/2015
21JGT01APRICOT, JAM, JELLY, PRESERVES, MARMALADE, BUTTER OR CANDIED
218LIST INGRE
3300ALLERGEN
New England District Office (NWE-DO)
3/17/2003
46YY99FOOD ADDITIVES FOR HUMAN USE, N.E.C.
11UNSAFE COL
218LIST INGRE
New Orleans District Office (NOL-DO)
1/17/2003
37JCT99SAUCES, N.E.C.
83NO PROCESS
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is Cottage Delight Limited's FDA import refusal history?

Cottage Delight Limited (FEI: 3008446202) has 6 FDA import refusal record(s) in our database, spanning from 1/17/2003 to 1/31/2015.

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. Cottage Delight Limited's FEI number is 3008446202.

What types of violations has Cottage Delight Limited received?

Cottage Delight Limited 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 Cottage Delight Limited come from?

All FDA import refusal data for Cottage Delight 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.