Wonderturn Ltd.
⚠️ Moderate Risk
FEI: 3000949344 • Wembley, Middlesex • UNITED KINGDOM
FEI Number
3000949344
Location
Wembley, Middlesex
Country
UNITED KINGDOMAddress
Trinity House, Heather Park Dr, Wembley, 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).
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).
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.
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.
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.
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)).
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).
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).
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.
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
| Date | Product | Violations | Division |
|---|---|---|---|
| 8/16/2012 | 65RBZ18SODIUM BICARBONATE (REPLENISHER) | 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. | New York District Office (NYK-DO) | |
| 12/10/2010 | 20DCT99BERRY JUICE, N.E.C. BERRY JUICE OR CONCENTRATES | 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) | 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.