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Wonderturn Ltd.

⚠️ Moderate Risk

FEI: 3000949344 • Wembley, Middlesex • UNITED KINGDOM

FEI

FEI Number

3000949344

📍

Location

Wembley, Middlesex

🇬🇧
🏢

Address

Trinity House, Heather Park Dr, Wembley, Middlesex, United Kingdom

Moderate Risk

FDA Import Risk Assessment

41.5
LowModerateHighCritical

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

Statistics

13
Total Refusals
11
Unique Violations
8/16/2012
Latest Refusal
12/13/2001
Earliest Refusal

Score Breakdown

Violation Severity
68.8×40%
Refusal Volume
42.5×30%
Recency
0.0×20%
Frequency
12.2×10%
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

113×

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).

1183×

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).

2742×

COLOR LBLG

The article appears to contain an artificial coloring and it fails to bear labeling stating that fact.

2382×

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.

91×

SALMONELLA

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain Salmonella, a poisonous and deleterious substance which may render it injurious to health.

161×

DIRECTIONS

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it is a device whose label appears to not bear adequate directions for use.

3241×

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)).

621×

NEEDS FCE

It appears the manufacturer is not registered as a low acid canned food or acidified food manufacturer pursuant to 21 CFR 108.25(c)(1) or 108.35(c)(1).

751×

UNAPPROVED

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a new drug within the meaning of Section 201(p) without an approved New Drug Application (NDA).

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.

2181×

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.

Refusal History

DateProductViolationsDivision
8/16/2012
65RBZ18SODIUM BICARBONATE (REPLENISHER)
118NOT LISTED
16DIRECTIONS
New York District Office (NYK-DO)
7/11/2011
28FGT03FIVE SPICE MIX, GROUND, CRACKED, WITHOUT SALT
218LIST INGRE
New York District Office (NYK-DO)
12/10/2010
07BGT99FRIED SNACK FOODS, N.E.C.
11UNSAFE COL
274COLOR LBLG
New York District Office (NYK-DO)
12/10/2010
20DCT99BERRY JUICE, N.E.C. BERRY JUICE OR CONCENTRATES
11UNSAFE COL
274COLOR LBLG
New York District Office (NYK-DO)
8/11/2010
26CCT99REFINED VEGETABLE OIL, SINGLE INGREDIENT, N.E.C.
75UNAPPROVED
Division of Northeast Imports (DNEI)
6/14/2010
28FGR03FIVE SPICE MIX, GROUND, CRACKED, WITHOUT SALT
9SALMONELLA
New York District Office (NYK-DO)
12/31/2008
02GFT11GRAM FLOUR
324NO ENGLISH
New York District Office (NYK-DO)
11/2/2007
28KGT99SPICES AND SEASONING, GROUND, CRACKED, WITH SALT, N.E.C.
11UNSAFE COL
New York District Office (NYK-DO)
9/22/2003
63HAA08CASTOR OIL (CATHARTIC)
118NOT LISTED
Chicago District Office (CHI-DO)
3/2/2003
24AEE10NAVY (WHITE) BEANS, (BAKED BEANS, PORK & BEANS)
62NEEDS FCE
83NO PROCESS
New York District Office (NYK-DO)
12/13/2001
26CCT11MUSTARD OIL, REFINED, SINGLE INGREDIENT, SEE 28O FOR MUSTARD OIL AS A FLAVORING
238UNSAFE ADD
New York District Office (NYK-DO)
12/13/2001
26CCT11MUSTARD OIL, REFINED, SINGLE INGREDIENT, SEE 28O FOR MUSTARD OIL AS A FLAVORING
238UNSAFE ADD
New York District Office (NYK-DO)
12/13/2001
65RBZ18SODIUM BICARBONATE (REPLENISHER)
118NOT LISTED
New York District Office (NYK-DO)

Frequently Asked Questions

What is Wonderturn Ltd.'s FDA import refusal history?

Wonderturn Ltd. (FEI: 3000949344) has 13 FDA import refusal record(s) in our database, spanning from 12/13/2001 to 8/16/2012.

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. Wonderturn Ltd.'s FEI number is 3000949344.

What types of violations has Wonderturn Ltd. received?

Wonderturn Ltd. has been cited for 11 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 Wonderturn Ltd. come from?

All FDA import refusal data for Wonderturn 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.